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 9:91724248 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000566

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_059_ROR2_602337_0002, 10984

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

9:g.91724248C>T
ENST00000550066.3:n.2714G>A
ENST00000375715.3:c.1826G>A
ENSP00000364867.1:p.Trp609Ter
ENST00000375708.3:c.2246G>A
ENSP00000364860.3:p.Trp749Ter

Variation displays