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 9:91724334 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002104 ; PhenCode KinMutBase_ROR2_DNA:g.226829G>A (C/T)

Most severe consequence
Clinical significance

Synonyms

LSDB 10988

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

9:g.91724334C>T
ENST00000550066.2:n.2628G>A
ENST00000375715.2:c.1740G>A
ENSP00000364867.1:p.Trp580Ter
ENST00000375708.3:c.2160G>A
ENSP00000364860.3:p.Trp720Ter

Variation displays