Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:111958657 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021678

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11390, 2010_April_001_304_SDHD_602690_0023

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

11:g.111958657G>A
ENST00000528182.1:c.129G>A
ENSP00000435475.1:p.Trp43Ter
ENST00000525987.1:n.134G>A
ENST00000526592.1:c.129G>A
ENSP00000432005.1:p.Trp43Ter
HG388_HG400_PATCH:g.111958656G>A
ENST00000532699.1:c.129G>A
ENSP00000456434.1:p.Trp43Ter
ENST00000375549.3:c.129G>A
ENSP00000364699.3:p.Trp43Ter
ENST00000525291.1:c.53-934G>A
ENST00000528021.1:c.129G>A
ENSP00000432465.1:p.Trp43Ter
ENST00000531744.1:c.129G>A
ENSP00000456957.1:p.Trp43Ter
ENST00000530923.1:c.119G>A
ENSP00000432946.1:p.Trp40Ter
ENST00000528048.1:c.129G>A
ENSP00000436217.1:p.Trp43Ter

Variation displays