Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome 12:25227346 (forward strand)|View in location tab

Co-located variants

COSMIC COSM4384681, COSM4384680 ; HGMD-PUBLIC CM061080, CM092327

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_077_KRAS_190070_0009, 5691, 5702

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 7 phenotypes.

Variant displays