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 5:132384154 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002860

Most severe consequence
Clinical significance

Synonyms

LSDB 11843

This variation has 9 HGVS names - click the plus to show

5:g.132384154C>T
ENST00000245407.4:c.505C>T
ENSP00000245407.3:p.Arg169Trp
ENST00000437841.3:c.394-1174C>T
ENST00000435065.3:c.577C>T
ENSP00000402760.2:p.Arg193Trp
ENST00000461013.2:n.7927C>T
ENST00000415928.2:c.274C>T
ENSP00000388838.1:p.Arg92Trp

Variation displays