Original source

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

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

Chromosome 14:75176389 (forward strand) | View in location tab

Co-located

with COSMIC COSM553691 (G/A)

Most severe consequence
Synonyms

Uniprot VAR_012051

This variation has 7 HGVS names - click the plus to show

Variation displays