Original source

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

Alleles
T/A/C|Ancestral: T|Ambiguity code: H
Location

Chromosome 12:25209904 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1676793 ; HGMD-PUBLIC CM061083

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5692, 2010_April_001_078_KRAS_190070_0010, 27631, SCV000061943

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and is associated with 7 phenotypes.

Variant displays