Original source

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

G/C/T | Ancestral: G | Ambiguity code: B

Chromosome 12:25227343 (forward strand) | View in location tab


with COSMIC COSM1159597 (G/T), COSM549 (G/T), COSM550 (G/C)

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 8 transcripts.

Variation displays