Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M
Location

Chromosome 12:25209907 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM061830

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5696, 2010_April_001_082_KRAS_190070_0014

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 2 phenotypes.

Variant displays