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 10:73375330 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074088

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13257

This variation has 13 HGVS names - click the plus to show

10:g.73375330G>A
ENST00000398809.4:c.902G>A
ENSP00000381789.4:p.Arg301Gln
ENST00000461841.3:c.1037G>A
ENSP00000473454.1:p.Arg346Gln
ENST00000224721.6:c.917G>A
ENSP00000224721.6:p.Arg306Gln
ENST00000466757.3:c.273G>A
ENSP00000473539.1:p.Arg92Gln
ENST00000398842.3:c.902G>A
ENSP00000381822.3:p.Arg301Gln
ENST00000299366.7:c.1037G>A
ENSP00000299366.7:p.Arg346Gln

Variation displays