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 10:93777592 (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 7 HGVS names - click the plus to show

10:g.93777592C>T
ENST00000371413.3:c.406C>T
ENSP00000360467.3:p.Arg136Trp
ENST00000464250.1:n.36C>T
ENST00000485458.1:n.321C>T
ENST00000371418.5:c.406C>T
ENSP00000360472.4:p.Arg136Trp

Variation displays