16-68737424-T-A
Variant summary
Our verdict is Likely benign. Variant got -5 ACMG points: 2P and 7B. PM2BP4_StrongBP6_ModerateBP7
The NM_004360.5(CDH1):c.9T>A(p.Pro3=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★). Synonymous variant affecting the same amino acid position (i.e. P3P) has been classified as Likely benign.
Frequency
Consequence
NM_004360.5 synonymous
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Likely_benign. Variant got -5 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
CDH1 | NM_004360.5 | c.9T>A | p.Pro3= | synonymous_variant | 1/16 | ENST00000261769.10 | |
CDH1 | NM_001317184.2 | c.9T>A | p.Pro3= | synonymous_variant | 1/15 | ||
CDH1 | NM_001317185.2 | c.-1607T>A | 5_prime_UTR_variant | 1/16 | |||
CDH1 | NM_001317186.2 | c.-1811T>A | 5_prime_UTR_variant | 1/15 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
CDH1 | ENST00000261769.10 | c.9T>A | p.Pro3= | synonymous_variant | 1/16 | 1 | NM_004360.5 | P1 | |
CDH1 | ENST00000422392.6 | c.9T>A | p.Pro3= | synonymous_variant | 1/15 | 1 | |||
CDH1 | ENST00000566612.5 | c.9T>A | p.Pro3= | synonymous_variant, NMD_transcript_variant | 1/15 | 1 | |||
CDH1 | ENST00000566510.5 | c.9T>A | p.Pro3= | synonymous_variant, NMD_transcript_variant | 1/15 | 5 |
Frequencies
GnomAD3 genomes Cov.: 33
GnomAD4 exome Data not reliable, filtered out with message: AC0 AF: 0.00 AC: 0AN: 1381862Hom.: 0 Cov.: 30 AF XY: 0.00 AC XY: 0AN XY: 682206
GnomAD4 genome Cov.: 33
ClinVar
Submissions by phenotype
Hereditary cancer-predisposing syndrome Benign:1
Likely benign, criteria provided, single submitter | clinical testing | Ambry Genetics | Aug 23, 2022 | This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity. - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.