Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A/C|Ancestral: G|Ambiguity code: V

Chromosome 11:2160956 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3931294, COSM3931293 ; HGMD-PUBLIC CM082897

Most severe consequence
Missense variant
Evidence status

Clinical significance


Uniprot VAR_063721

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 36 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays