Original source

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

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

Chromosome 6:3105685 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_041042

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays