Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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 COSM506 (T/G), COSM24602 (T/A) ; HGMD-PUBLIC CM070963

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5699, 2010_April_001_084_KRAS_190070_0017

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

Variation displays