17-43094176-A-T

Variant names:

• chr17-43094176-A-T
• rs878854932
• NM_007294.4:c.1355T>A

Variant summary

Our verdict is Uncertain significance. The variant received 1 ACMG points: 2P and 1B. PM2 BP6

The NM_007294.4(BRCA1):​c.1355T>A​(p.Val452Glu) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. V452I) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: BRCA1 NM_007294.4 missense
• Clinical Significance: Conflicting classifications of pathogenicity criteria provided, conflicting classifications U:1 B:1
• Conservation: PhyloP100: -0.0740
• Publications: 0 publications found

Genes affected

BRCA1 (HGNC:1100): (BRCA1 DNA repair associated) This gene encodes a 190 kD nuclear phosphoprotein that plays a role in maintaining genomic stability, and it also acts as a tumor suppressor. The BRCA1 gene contains 22 exons spanning about 110 kb of DNA. The encoded protein combines with other tumor suppressors, DNA damage sensors, and signal transducers to form a large multi-subunit protein complex known as the BRCA1-associated genome surveillance complex (BASC). This gene product associates with RNA polymerase II, and through the C-terminal domain, also interacts with histone deacetylase complexes. This protein thus plays a role in transcription, DNA repair of double-stranded breaks, and recombination. Mutations in this gene are responsible for approximately 40% of inherited breast cancers and more than 80% of inherited breast and ovarian cancers. Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene. Many alternatively spliced transcript variants, some of which are disease-associated mutations, have been described for this gene, but the full-length natures of only some of these variants has been described. A related pseudogene, which is also located on chromosome 17, has been identified. [provided by RefSeq, May 2020]

BRCA1 Gene-Disease associations (from GenCC):

• breast-ovarian cancer, familial, susceptibility to, 1

  Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: Ambry Genetics, ClinGen, Labcorp Genetics (formerly Invitae), Genomics England PanelApp
• Fanconi anemia, complementation group S

  Inheritance: AR Classification: DEFINITIVE, STRONG, MODERATE, LIMITED Submitted by: G2P, Labcorp Genetics (formerly Invitae), ClinGen, Ambry Genetics
• pancreatic cancer, susceptibility to, 4

  Inheritance: AD Classification: MODERATE Submitted by: Genomics England PanelApp
• hereditary breast ovarian cancer syndrome

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• Fanconi anemia

  Inheritance: AR Classification: SUPPORTIVE Submitted by: Orphanet

ACMG classification

Our verdict: Uncertain_significance. The variant received 1 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP6: Variant 17-43094176-A-T is Benign according to our data. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692. Variant chr17-43094176-A-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 1770692.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
BRCA1	NM_007294.4	c.1355T>A	p.Val452Glu	missense_variant	Exon 10 of 23	ENST00000357654.9	NP_009225.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
BRCA1	ENST00000357654.9	c.1355T>A	p.Val452Glu	missense_variant	Exon 10 of 23	1	NM_007294.4	ENSP00000350283.3

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 34

GnomAD4 genome Cov.: 32

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Uncertain:1 Benign:1

Revision: criteria provided, conflicting classifications

Submissions by phenotype

Hereditary cancer-predisposing syndrome Uncertain:1 Benign:1

Oct 31, 2021

Ambry Genetics

Significance: Uncertain significance

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The p.V452E variant (also known as c.1355T>A), located in coding exon 9 of the BRCA1 gene, results from a T to A substitution at nucleotide position 1355. The valine at codon 452 is replaced by glutamic acid, an amino acid with dissimilar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. -

Mar 23, 2023

University of Washington Department of Laboratory Medicine, University of Washington

Significance: Likely benign

Review Status: criteria provided, single submitter

Collection Method: curation

Missense variant in a coldspot region where missense variants are very unlikely to be pathogenic (PMID:31911673). -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
AlphaMissense	Benign	0.16
BayesDel_addAF	Pathogenic	0.24	D
BayesDel_noAF	Uncertain	0.11
CADD	Benign	16
DANN	Benign	0.96
DEOGEN2	Uncertain	0.61	D;.;.;.;T;T;.;.;T
Eigen	Benign	-0.39
Eigen_PC	Benign	-0.62
FATHMM_MKL	Benign	0.068	N
LIST_S2	Benign	0.82	T;T;T;T;T;T;T;T;T
M_CAP	Uncertain	0.18	D
MetaRNN	Uncertain	0.49	T;T;T;T;T;T;T;T;T
MetaSVM	Benign	-0.74	T
MutationAssessor	Pathogenic	3.0	M;M;.;.;.;.;.;.;.
PhyloP100		-0.074
PrimateAI	Benign	0.25	T
PROVEAN	Pathogenic	-4.7	D;D;D;D;.;D;D;D;D
REVEL	Uncertain	0.58
Sift	Uncertain	0.0010	D;D;D;D;.;D;D;D;D
Sift4G	Benign	0.15	T;T;T;T;.;T;.;D;D
Polyphen		0.99	D;.;.;D;.;.;.;.;.
Vest4		0.54
MutPred		0.50		Gain of helix (P = 0.0034);Gain of helix (P = 0.0034);.;Gain of helix (P = 0.0034);.;Gain of helix (P = 0.0034);.;.;Gain of helix (P = 0.0034);
MVP		0.79
MPC		0.54
ClinPred		0.82	D
GERP RS		1.0
Varity_R		0.40
gMVP		0.35

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs878854932; hg19: chr17-41246193;