R108T (p.Arg108Thr) variant of FERMT1 (Fermitin family homolog 1)
R108T (p.Arg108Thr) in FERMT1 (Fermitin family homolog 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 0.36 / 1. The record also includes population frequency data, published literature, and structural context.
R108T (p.Arg108Thr) variant details
- p.Arg108Thr
- rs201129798
- ClinGen CA9758490
- ClinVar RCV002046831
- ClinVar RCV005841849
- Uncertain significance
- not provided; Inborn genetic diseases
- Missense
- Variant Prioritization Score for Impact Estimate 0.363
- REVEL 0.15
- CADD 21.80
- PolyPhen-2 0.46
- SIFT 0.35
- ClinVar: Uncertain significance (not provided; Inborn genetic diseases)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the REMAINING population (allele frequency 0.00048)
- 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)