Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 12:25245345 (forward strand) | View in location tab


with COSMIC COSM1360883 (C/T), COSM12722 (C/T) ; HGMD-PUBLIC CM061082

Most severe consequence
Evidence status

Clinical significance


LSDB NG_007524.1:g.10576G>A, 2010_April_001_080_KRAS_190070_0012, 5694

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variation displays