P87T (p.Pro87Thr) variant of ACVR1 (Activin receptor type-1)
P87T (p.Pro87Thr) in ACVR1 (Activin receptor type-1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Inborn genetic diseases; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data, published literature, and structural context.
P87T (p.Pro87Thr) variant details
- p.Pro87Thr
- rs1686461170
- ClinGen CA349193577
- ClinVar RCV002981804
- ClinVar RCV005099021
- Uncertain significance
- Inborn genetic diseases; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.441
- REVEL 0.25
- CADD 19.40
- PolyPhen-2 0.01
- SIFT 0.49
- ClinVar: Uncertain significance (Inborn genetic diseases; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Latino/Admixed American population (allele frequency 4.5e-05)
- 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)