A75S (p.Ala75Ser) variant of RAI1 (Retinoic acid-induced protein 1)
A75S (p.Ala75Ser) in RAI1 (Retinoic acid-induced protein 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as benign/likely benign in the context of Inborn genetic diseases; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data, published literature, and structural context.
A75S (p.Ala75Ser) variant details
- p.Ala75Ser
- rs566875015
- ClinGen CA8418078
- cosmic curated COSV55395
- ClinVar RCV001615036
- Benign/Likely benign
- Inborn genetic diseases; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.0666
- REVEL 0.01
- ESM-1b 0.00
- AlphaMissense 0.08
- CADD 5.46
- PolyPhen-2 0.05
- SIFT 0.10
- ClinVar: Benign/Likely benign (Inborn genetic diseases; not provided)
- EBI: Benign
- UniProt: Benign
- Most common in the HGDP:SINDHI population (allele frequency 0.024)
- 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)