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 17:50185606 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1710464

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 1 sample genotype and is mentioned in 1 citation.

Variant displays