Original source

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

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

Chromosome 11:112086940 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM092194, CM020973

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11392, 2010_April_001_305_SDHD_602690_0025

This variation has 22 HGVS names - click the plus to show

11:g.112086940C>A
ENST00000528182.2:c.33C>A
ENSP00000435475.1:p.Cys11Ter
ENST00000525987.2:n.38C>A
ENST00000526592.2:c.33C>A
ENSP00000432005.1:p.Cys11Ter
ENST00000614349.1:c.33C>A
ENSP00000480666.1:p.Cys11Ter
ENST00000532699.1:c.33C>A
ENSP00000456434.1:p.Cys11Ter
ENST00000375549.4:c.33C>A
ENSP00000364699.3:p.Cys11Ter
ENST00000528021.2:c.33C>A
ENSP00000432465.1:p.Cys11Ter
ENST00000525291.2:c.33C>A
ENSP00000436669.1:p.Cys11Ter
ENST00000530923.2:c.23C>A
ENSP00000432946.1:p.Cys8Ter
ENST00000531744.2:c.33C>A
ENSP00000456957.1:p.Cys11Ter
ENST00000528048.2:c.33C>A
ENSP00000436217.1:p.Cys11Ter

Variation displays