Original source

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

Alleles
G/A/T|Ancestral: G|Ambiguity code: D
Location

Chromosome 7:128254587 (forward strand)|View in location tab

Co-located variants

COSMIC COSM2768806 ; HGMD-PUBLIC CM981201

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_011955

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2 sample genotypes.

Variant displays