Original source

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

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

Chromosome 8:43037305 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065262

Most severe consequence
Clinical significance

Synonyms

LSDB 16749

This variation has 14 HGVS names - click the plus to show

8:g.43037305C>T
ENST00000522082.1:c.271C>T
ENSP00000430151.1:p.Arg91Cys
ENST00000521576.1:c.181C>T
ENSP00000429029.1:p.Arg61Cys
ENST00000458501.2:c.1114C>T
ENSP00000389524.2:p.Arg372Cys
ENST00000519000.1:n.516C>T
ENST00000379644.4:c.1030C>T
ENSP00000368965.4:p.Arg344Cys
ENST00000297798.7:c.226C>T
ENSP00000297798.7:p.Arg76Cys
ENST00000524016.1:c.134C>T
ENSP00000428322.1:p.Arg46Cys

Variation displays