E26Q (p.Glu26Gln) variant of TCF7L2 (Transcription factor 7-like 2)
E26Q (p.Glu26Gln) in TCF7L2 (Transcription factor 7-like 2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E26Q (p.Glu26Gln) variant details
- p.Glu26Gln
- NCI-TCGA Cosmic COSV6050
- cosmic curated COSV60503
- Ensembl rs2134177358
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available