Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D
Location

Chromosome 6:159907580 (forward strand)|View in location tab

Co-located variant

COSMIC COSM4996670

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays