S16G (p.Ser16Gly) variant of TERT (Telomerase reverse transcriptase)
S16G (p.Ser16Gly) in TERT (Telomerase reverse transcriptase) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Dyskeratosis congenita. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
S16G (p.Ser16Gly) variant details
- p.Ser16Gly
- rs2126692725
- ClinGen CA359059790
- ClinVar RCV004559384
- Ensembl rs2126692725
- Uncertain significance
- Dyskeratosis congenita
- Missense
- Variant Prioritization Score for Impact Estimate 0.152
- REVEL 0.09
- MetaLR 0.34
- MetaSVM -0.69
- CADD 10.10
- PolyPhen-2 0.00
- SIFT 0.95
- ClinVar: Uncertain significance (Dyskeratosis congenita)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available
- Cited in: Dyskeratosis Congenita and Related Telomere Biology Disorders. (PMID 20301779)
- Cited in: Cancer Genetics Risk Assessment and Counseling (PDQ®): Health Professional Version. (PMID 26389258)