Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 17:42901105 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960668

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6320, 2010_April_001_054_G6PC_232200_0007

This variation has 11 HGVS names - click the plus to show

17:g.42901105T>C
ENST00000585489.1:c.229T>C
ENSP00000466202.1:p.Trp77Arg
ENST00000588481.1:n.294T>C
ENST00000253801.3:c.229T>C
ENSP00000253801.1:p.Trp77Arg
ENST00000592383.2:c.229T>C
ENSP00000465958.1:p.Trp77Arg
LRG_147:g.5308T>C
LRG_147t1.1:c.229T>C
LRG_147p1.1:p.Trp77Arg

Variation displays