A3T (p.Ala3Thr) variant of ID3 (Q02535)
A3T (p.Ala3Thr) in ID3 (Q02535) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.73 / 1. The record also includes population frequency data.
A3T (p.Ala3Thr) variant details
- p.Ala3Thr
- rs1381240589
- NCI-TCGA Cosmic COSV6580
- gnomAD rs1381240589
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.734
- REVEL 0.70
- MetaLR 0.69
- MetaSVM 0.46
- CADD 28.00
- PolyPhen-2 1.00
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the African/African-American population (allele frequency 2.4e-05)