D42N (p.Asp42Asn) variant of HNRNPA1 (P09651)
D42N (p.Asp42Asn) in HNRNPA1 (P09651) 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 0.69 / 1. The record also includes structural context.
D42N (p.Asp42Asn) variant details
- p.Asp42Asn
- rs61910737
- NCI-TCGA Cosmic COSV5293
- cosmic curated COSV52938
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.69
- AlphaMissense 0.98
- MetaLR 0.73
- MetaSVM 0.60
- PolyPhen-2 0.93
- SIFT 0.01
- EVE 0.42
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available