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 11:111958592 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013282

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11379, 2010_April_001_299_SDHD_602690_0012

This variation has 20 HGVS names - click the plus to show

11:g.111958592C>T
ENST00000528182.1:c.64C>T
ENSP00000435475.1:p.Arg22Ter
ENST00000525987.1:n.69C>T
ENST00000526592.1:c.64C>T
ENSP00000432005.1:p.Arg22Ter
HG388_HG400_PATCH:g.111958591C>T
ENST00000532699.1:c.64C>T
ENSP00000456434.1:p.Arg22Ter
ENST00000375549.3:c.64C>T
ENSP00000364699.3:p.Arg22Ter
ENST00000525291.1:c.52+909C>T
ENST00000528021.1:c.64C>T
ENSP00000432465.1:p.Arg22Ter
ENST00000531744.1:c.64C>T
ENSP00000456957.1:p.Arg22Ter
ENST00000530923.1:c.54C>T
ENSP00000432946.1:p.Arg19Ter
ENST00000528048.1:c.64C>T
ENSP00000436217.1:p.Arg22Ter

Variation displays