Original source

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

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

Chromosome 10:13288428 (forward strand) | View in location tab

Co-located

with COSMIC COSM916259 (C/T) ; HGMD-PUBLIC CM001297

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

10:g.13288428C>T
ENST00000396913.3:c.310G>A
ENSP00000380121.2:p.Gly104Ser
ENST00000453759.3:c.310G>A
ENSP00000412525.2:p.Gly104Ser
ENST00000396920.4:c.559G>A
ENSP00000380126.3:p.Gly187Ser
ENST00000479604.1:c.616G>A
ENSP00000420117.1:p.Gly206Ser
ENST00000263038.5:c.610G>A
ENSP00000263038.4:p.Gly204Ser

Variation displays