Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 3:41224613 (forward strand) | View in location tab

Co-located

with COSMIC COSM5670 (G/T), COSM5671 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

This variation has 40 HGVS names - click the plus to show

Variation displays