Original source

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

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

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

Co-located

with COSMIC COSM24602 (T/A), COSM506 (T/G) ; HGMD-PUBLIC CM070963

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5699, 2010_April_001_084_KRAS_190070_0017

This variant has 9 HGVS names - click the plus to show

About this variant

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

Variant displays