Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W
Location

Chromosome 12:25245370 (forward strand)|View in location tab

Co-located variants

COSMIC COSM506, COSM24602 ; HGMD-PUBLIC CM070963

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5699, 2010_April_001_084_KRAS_190070_0017

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variant displays