Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

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

Co-located

with HGMD-PUBLIC CM981201

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_011955

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2 sample genotypes.

Variant displays