Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.26 (T)

Chromosome 11:17388025 (forward strand) | View in location tab


with COSMIC COSM3765554 (T/C) ; HGMD-PUBLIC CM981121

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 9 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2537 sample genotypes, is associated with 8 phenotypes and is mentioned in 102 citations.

Variant displays