Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 17:42909353 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM001694, CM950487

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_060_G6PC_232200_0014, 6327

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

17:g.42909353T>G
ENST00000585489.1:c.447-1562T>G
ENST00000592383.3:c.420T>G
ENSP00000465958.1:p.Cys140Trp
ENST00000253801.4:c.497T>G
ENSP00000253801.1:p.Val166Gly
LRG_147:g.13556T>G
LRG_147t1:c.497T>G
LRG_147p1:p.Val166Gly

Variation displays