Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)
Location

Chromosome 16:88646131 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960428 ; PhenCode CYBAbase_D0024:g.5911C>A (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

Variant allele A
16:g.88646131G>A
ENST00000567174.2:c.354C>T
ENST00000563526.2:n.886C>T
ENST00000569359.2:c.354C>T
ENST00000566229.1:c.343C>T
ENSP00000457060.1:p.Arg115Trp
ENST00000565588.2:c.138C>T
ENSP00000455537.1:p.Arg47Trp
ENST00000261623.4:c.354C>T
ENST00000566534.2:n.933C>T
LRG_52:g.9919C>T
LRG_52t1.1:c.354C>T

Variant allele T
16:g.88646131G>T
ENST00000567174.2:c.354C>A
ENSP00000454951.1:p.Ser118Arg
ENST00000563526.2:n.886C>A
ENST00000569359.2:c.354C>A
ENSP00000456079.1:p.Ser118Arg
ENST00000566229.1:c.343C>A
ENST00000565588.2:c.138C>A
ENST00000261623.4:c.354C>A
ENSP00000261623.3:p.Ser118Arg
ENST00000566534.2:n.933C>A
LRG_52:g.9919C>A
LRG_52t1.1:c.354C>A
LRG_52p1.1:p.Ser118Arg

Variation displays