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 9:94486529 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM032028

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_058_ROR2_602337_0002, 22351

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

9:g.94486529C>T
ENST00000550066.1:n.2715G>A
ENST00000375715.1:c.1827G>A
ENSP00000364867.1:p.Trp609Ter
ENST00000375708.3:c.2247G>A
ENSP00000364860.3:p.Trp749Ter

Variation displays