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 17:41061424 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960671, CM990610

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6324, 2010_April_001_057_G6PC_232200_0011

This variation has 9 HGVS names - click the plus to show

17:g.41061424G>A
ENST00000585489.1:c.447-1508G>A
ENST00000592383.1:c.474G>A
ENSP00000465958.1:p.Trp158Ter
ENST00000253801.2:c.551G>A
ENSP00000253801.1:p.Gly184Glu
LRG_147:g.13610G>A
LRG_147t1.1:c.551G>A
LRG_147p1.1:p.Gly184Glu

Variation displays