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 14:75176389 (forward strand)|View in location tab

Co-located variant

COSMIC COSM553691

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_012051

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and 1 regulatory feature.

Variant displays