rs121912741
Variant summary
Our verdict is Pathogenic. Variant got 10 ACMG points: 10P and 0B. PM1PM2PM5PP3_ModeratePP5_Moderate
The NM_000342.4(SLC4A1):c.2312G>T(p.Gly771Val) variant causes a missense, splice region change. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a pathogenic outcome for this variant. 2/3 splice prediction tools predicting alterations to normal splicing. Variant has been reported in ClinVar as Likely pathogenic (★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. G771D) has been classified as Pathogenic.
Frequency
Consequence
NM_000342.4 missense, splice_region
Scores
Clinical Significance
Conservation
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ACMG classification
Verdict is Pathogenic. Variant got 10 ACMG points.
Transcripts
RefSeq
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | MANE | UniProt |
---|---|---|---|---|---|---|---|
SLC4A1 | NM_000342.4 | c.2312G>T | p.Gly771Val | missense_variant, splice_region_variant | 18/20 | ENST00000262418.12 | |
SLC4A1 | XM_011525129.3 | c.2222G>T | p.Gly741Val | missense_variant, splice_region_variant | 17/19 | ||
SLC4A1 | XM_005257593.6 | c.2117G>T | p.Gly706Val | missense_variant, splice_region_variant | 16/18 | ||
SLC4A1 | XM_011525130.2 | c.*22G>T | 3_prime_UTR_variant | 18/18 |
Ensembl
Gene | Transcript | HGVSc | HGVSp | Effect | #exon/exons | TSL | MANE | Appris | UniProt |
---|---|---|---|---|---|---|---|---|---|
SLC4A1 | ENST00000262418.12 | c.2312G>T | p.Gly771Val | missense_variant, splice_region_variant | 18/20 | 1 | NM_000342.4 | P1 | |
SLC4A1 | ENST00000399246.3 | c.1214G>T | p.Gly405Val | missense_variant, splice_region_variant | 13/15 | 5 |
Frequencies
GnomAD3 genomes Cov.: 32
GnomAD4 exome Cov.: 33
GnomAD4 genome Cov.: 32
ClinVar
Submissions by phenotype
Hereditary spherocytosis type 4 Pathogenic:1
Likely pathogenic, criteria provided, single submitter | clinical testing | UOS Fisiopatologia delle Anemie, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milano | Nov 25, 2019 | - - |
Computational scores
Source:
Splicing
Find out detailed SpliceAI scores and Pangolin per-transcript scores at
Publications
No publications associated with this variant yet.