Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K
Location

Chromosome 9:711384 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_026212

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2 sample genotypes.

Variant displays