D11N (p.Asp11Asn) variant of HNF4A (P41235)
D11N (p.Asp11Asn) in HNF4A (P41235) 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 0.36 / 1. The record also includes population frequency data and structural context.
D11N (p.Asp11Asn) variant details
- p.Asp11Asn
- rs200655531
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10029
- 1000Genomes rs200655531
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.362
- CADD 15.20
- SIFT 0.58
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available