Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with COSMIC COSM87288 (G/A) ; HGMD-PUBLIC CM061079

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5693, 2010_April_001_079_KRAS_190070_0011

This variant has 6 HGVS names - click the plus to show

About this variant

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

Variant displays