D151N (p.Asp151Asn) variant of RINL (Q6ZS11)
D151N (p.Asp151Asn) in RINL (Q6ZS11) 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 0.64 / 1. The record also includes population frequency data and structural context.
D151N (p.Asp151Asn) variant details
- p.Asp151Asn
- rs755164424
- NCI-TCGA Cosmic COSV6157
- cosmic curated COSV61574
- ExAC rs755164424
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.639
- CADD 32.00
- PolyPhen-2 0.11
- SIFT 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available