S2T (p.Ser2Thr) variant of RLBP1 (Retinaldehyde-binding protein 1)
S2T (p.Ser2Thr) in RLBP1 (Retinaldehyde-binding protein 1) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided; Inborn genetic diseases. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data, published literature, and structural context.
S2T (p.Ser2Thr) variant details
- p.Ser2Thr
- rs140569547
- ClinGen CA7722427
- ClinVar RCV001888818
- ClinVar RCV005472974
- Uncertain significance
- not provided; Inborn genetic diseases
- Missense
- Variant Prioritization Score for Impact Estimate 0.166
- REVEL 0.11
- CADD 14.30
- PolyPhen-2 0.00
- SIFT 0.15
- ClinVar: Uncertain significance (not provided; Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 1.8e-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)