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 12:25227351 (forward strand)|View in location tab

Co-located variants

COSMIC COSM87288 ; HGMD-PUBLIC CM061079

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5693, 2010_April_001_079_KRAS_190070_0011

HGVS names

This variant has 6 HGVS names - Show

About this variant

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

Variant displays