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
Location

Chromosome 5:74713584 (forward strand) | View in location tab

Co-located

with COSMIC COSM1070016 (C/T) ; HGMD-PUBLIC CM940931

Most severe consequence
Clinical significance

Synonyms

LSDB 14263

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

5:g.74713584C>T
ENST00000511181.2:c.175C>T
ENSP00000426285.1:p.Arg59Ter
ENST00000504459.2:n.47C>T
ENST00000261416.8:c.850C>T
ENSP00000261416.7:p.Arg284Ter

Variation displays