R74H (p.Arg74His) variant of SPTB (Spectrin beta chain, erythrocytic)
R74H (p.Arg74His) in SPTB (Spectrin beta chain, erythrocytic) 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 0.51 / 1. The record also includes population frequency data and published literature.
R74H (p.Arg74His) variant details
- p.Arg74His
- rs757763783
- ClinGen CA7231512
- NCI-TCGA Cosmic COSV6763
- cosmic curated COSV67633
- Uncertain significance
- Inborn genetic diseases; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.513
- MetaLR 0.12
- MetaSVM -0.94
- CADD 22.60
- PolyPhen-2 0.10
- SIFT 0.01
- ClinVar: Uncertain significance (Inborn genetic diseases; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence 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)