Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 4:146640335 (forward strand)|View in location tab

Co-located variant

COSMIC COSM447451

Most severe consequence
 
Missense variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays