Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 11:112086921 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM020972

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_306_SDHD_602690_0026, 11393

HGVS names

This variant has 22 HGVS names - Hide

11:g.112086921G>A
ENST00000528182.5:c.14G>A
ENSP00000435475.1:p.Trp5Ter
ENST00000525987.5:n.19G>A
ENST00000526592.5:c.14G>A
ENSP00000432005.1:p.Trp5Ter
ENST00000614349.4:c.14G>A
ENSP00000480666.1:p.Trp5Ter
ENST00000532699.1:c.14G>A
ENSP00000456434.1:p.Trp5Ter
ENST00000375549.7:c.14G>A
ENSP00000364699.3:p.Trp5Ter
ENST00000528021.5:c.14G>A
ENSP00000432465.1:p.Trp5Ter
ENST00000525291.5:c.14G>A
ENSP00000436669.1:p.Trp5Ter
ENST00000530923.5:c.4G>A
ENSP00000432946.1:p.Trp2Ter
ENST00000531744.5:c.14G>A
ENSP00000456957.1:p.Trp5Ter
ENST00000528048.5:c.14G>A
ENSP00000436217.1:p.Trp5Ter

About this variant

This variant overlaps 24 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays