Original source

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

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

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

Co-located

with COSMIC COSM1676793 (T/A) ; HGMD-PUBLIC CM061083

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5692, 2010_April_001_078_KRAS_190070_0010, 27631, SCV000061943

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and is associated with 3 phenotypes.

Variation displays