Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 17:50185606 (forward strand) | View in location tab

Co-located

with COSMIC COSM1710464 (T/C)

Most severe consequence
Evidence status

Synonyms

This variation has 6 HGVS names - click the plus to show

Variation displays