V79M (p.Val79Met) variant of IL2RB (P14784)
V79M (p.Val79Met) in IL2RB (P14784) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign/likely benign in the context of not specified; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data.
V79M (p.Val79Met) variant details
- p.Val79Met
- rs149508414
- ClinGen CA10216684
- ClinVar RCV000892425
- ClinVar RCV003920782
- Benign/Likely benign
- not specified; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.149
- REVEL 0.09
- CADD 7.11
- PolyPhen-2 0.03
- SIFT 0.21
- ClinVar: Benign/Likely benign (not specified; not provided)
- EBI: Benign
- UniProt: Benign
- Most common in the HGDP:YI population (allele frequency 0.05)