Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:94499682 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002099

Most severe consequence
Clinical significance

Synonyms

LSDB 10989

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

9:g.94499682G>A
ENST00000550066.1:n.1081C>T
ENST00000375715.1:c.193C>T
ENSP00000364867.1:p.Arg65Ter
ENST00000375708.3:c.613C>T
ENSP00000364860.3:p.Arg205Ter

Variation displays