Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.50 (C)
Location

Chromosome 17:75131588 (forward strand) | View in location tab

Co-located

with COSMIC COSM4130605 (T/C)

Most severe consequence
Evidence status

Synonyms

This variation has 10 HGVS names - click the plus to show

Variation displays