14-105855041-A-G
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Variant summary
Our verdict is Benign. Variant got -15 ACMG points: 0P and 15B. BP4_StrongBP6_ModerateBP7BA1
The ENST00000637539.2(IGHM):āc.843T>Cā(p.Thr281=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0171 in 778,228 control chromosomes in the GnomAD database, including 800 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (ā ).
Frequency
Genomes: š 0.049 ( 540 hom., cov: 33)
Exomes š: 0.0096 ( 260 hom. )
Consequence
IGHM
ENST00000637539.2 synonymous
ENST00000637539.2 synonymous
Scores
2
Clinical Significance
Conservation
PhyloP100: 0.0270
Genes affected
IGHM (HGNC:5541): (immunoglobulin heavy constant mu) Immunoglobulins (Ig) are the antigen recognition molecules of B cells. An Ig molecule is made up of 2 identical heavy chains and 2 identical light chains (see MIM 147200) joined by disulfide bonds so that each heavy chain is linked to a light chain and the 2 heavy chains are linked together. Each Ig heavy chain has an N-terminal variable (V) region containing the antigen-binding site and a C-terminal constant (C) region, encoded by an individual C region gene, that determines the isotype of the antibody and provides effector or signaling functions. The heavy chain V region is encoded by 1 each of 3 types of genes: V genes (see MIM 147070), joining (J) genes (see MIM 147010), and diversity (D) genes (see MIM 146910). The C region genes are clustered downstream of the V region genes within the heavy chain locus on chromosome 14. The IGHM gene encodes the C region of the mu heavy chain, which defines the IgM isotype. Naive B cells express the transmembrane forms of IgM and IgD (see IGHD; MIM 1471770) on their surface. During an antibody response, activated B cells can switch to the expression of individual downstream heavy chain C region genes by a process of somatic recombination known as isotype switching. In addition, secreted Ig forms that act as antibodies can be produced by alternative RNA processing of the heavy chain C region sequences. Although the membrane forms of all Ig isotypes are monomeric, secreted IgM forms pentamers, and occasionally hexamers, in plasma (summary by Janeway et al., 2005).[supplied by OMIM, Aug 2010]
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ACMG classification
Classification made for transcript
Verdict is Benign. Variant got -15 ACMG points.
BP4
Computational evidence support a benign effect (BayesDel_noAF=-0.88).
BP6
Variant 14-105855041-A-G is Benign according to our data. Variant chr14-105855041-A-G is described in ClinVar as [Benign]. Clinvar id is 810941.Status of the report is criteria_provided_single_submitter, 1 stars.
BP7
Synonymous conserved (PhyloP=0.027 with no splicing effect.
BA1
GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.156 is higher than 0.05.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
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Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
IGHM | ENST00000637539.2 | c.843T>C | p.Thr281= | synonymous_variant | 3/6 | A2 | |||
IGHM | ENST00000390559.6 | c.843T>C | p.Thr281= | synonymous_variant | 3/4 | P3 |
Frequencies
GnomAD3 genomes AF: 0.0484 AC: 7268AN: 150020Hom.: 531 Cov.: 33
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GnomAD3 exomes AF: 0.0146 AC: 3580AN: 245966Hom.: 220 AF XY: 0.0122 AC XY: 1636AN XY: 133662
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GnomAD4 exome AF: 0.00960 AC: 6032AN: 628138Hom.: 260 Cov.: 0 AF XY: 0.00851 AC XY: 2912AN XY: 342202
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GnomAD4 genome AF: 0.0485 AC: 7285AN: 150090Hom.: 540 Cov.: 33 AF XY: 0.0466 AC XY: 3412AN XY: 73226
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ClinVar
Significance: Benign
Submissions summary: Benign:1
Revision: criteria provided, single submitter
LINK: link
Submissions by phenotype
Autosomal recessive agammaglobulinemia 1 Benign:1
Benign, criteria provided, single submitter | clinical testing | ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories | Sep 13, 2022 | - - |
Computational scores
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BayesDel_noAF
Benign
CADD
Benign
DANN
Benign
Splicing
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Details are displayed if max score is > 0.2
Find out detailed SpliceAI scores and Pangolin per-transcript scores at