Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 12:25245284 (forward strand) | View in location tab

Co-located

with COSMIC COSM1360859 (G/A), COSM1168054 (G/T) ; HGMD-PUBLIC CM070968, CM070967, CM061081

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_081_KRAS_190070_0013, 5695

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

Variation displays