Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 14:23424842 (forward strand) | View in location tab

Co-located

with COSMIC COSM4050071 (C/T) ; HGMD-PUBLIC HM971868

Most severe consequence
Synonyms

Uniprot VAR_042810

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

Variation displays