Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 9:91724990 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002102 ; PhenCode KinMutBase_ROR2_DNA:g.226173C>T (G/A)

Most severe consequence
Clinical significance

Synonyms

LSDB 10986

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

9:g.91724990G>A
ENST00000550066.3:n.1972C>T
ENST00000375715.3:c.1084C>T
ENSP00000364867.1:p.Gln362Ter
ENST00000375708.3:c.1504C>T
ENSP00000364860.3:p.Gln502Ter

Variation displays