M57V (p.Met57Val) variant of EPAS1 (Q99814)
M57V (p.Met57Val) in EPAS1 (Q99814) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data, published literature, and structural context.
M57V (p.Met57Val) variant details
- p.Met57Val
- rs1684043368
- ClinGen CA346697177
- ClinVar RCV002414684
- Ensembl rs1684043368
- Uncertain significance
- Inborn genetic diseases
- Missense
- Variant Prioritization Score for Impact Estimate 0.555
- REVEL 0.60
- MetaLR 0.11
- MetaSVM -0.98
- CADD 25.10
- PolyPhen-2 0.78
- SIFT 0.00
- ClinVar: Uncertain significance (Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available
- Cited in: Specific guidelines for assessing and improving the methodological quality of economic evaluations of newborn screening. (PMID 22947299)
- Cited in: Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and… (PMID 23037933)