Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 11:111958623 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013790

Most severe consequence
Clinical significance

Synonyms

LSDB 2010_April_001_297_SDHD_602690_0008

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

11:g.111958623C>A
ENST00000528182.1:c.95C>A
ENSP00000435475.1:p.Ser32Ter
ENST00000525987.1:n.100C>A
ENST00000526592.1:c.95C>A
ENSP00000432005.1:p.Ser32Ter
HG388_HG400_PATCH:g.111958622C>A
ENST00000532699.1:c.95C>A
ENSP00000456434.1:p.Ser32Ter
ENST00000375549.3:c.95C>A
ENSP00000364699.3:p.Ser32Ter
ENST00000525291.1:c.52+940C>A
ENST00000528021.1:c.95C>A
ENSP00000432465.1:p.Ser32Ter
ENST00000530923.1:c.85C>A
ENSP00000432946.1:p.Ser29Ter
ENST00000531744.1:c.95C>A
ENSP00000456957.1:p.Ser32Ter
ENST00000528048.1:c.95C>A
ENSP00000436217.1:p.Ser32Ter

Variation displays