Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 10:95537349 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073177

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 12772

This variation has 8 HGVS names - click the plus to show

10:g.95537349C>T
ENST00000542308.1:c.288-12507C>T
ENST00000371413.3:c.406C>T
ENSP00000360467.3:p.Arg136Trp
ENST00000464250.1:n.36C>T
ENST00000485458.1:n.321C>T
ENST00000371418.4:c.406C>T
ENSP00000360472.4:p.Arg136Trp

Variation displays