Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 9:91724247 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM032028

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_058_ROR2_602337_0002, 22351

HGVS names

This variant has 6 HGVS names - Hide

9:g.91724247C>T
ENST00000550066.5:n.2715G>A
ENST00000375715.5:c.1827G>A
ENSP00000364867.1:p.Trp609Ter
ENST00000375708.3:c.2247G>A
ENSP00000364860.3:p.Trp749Ter

About this variant

This variant overlaps 3 transcripts and is associated with 3 phenotypes.

Variant displays