Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 11:112088939 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM000207, CD094779

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11370, NM_003002.1:c.242C>T, 2010_April_001_293_SDHD_602690_0003

HGVS names

This variant has 23 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, is associated with 6 phenotypes and is mentioned in 6 citations.

Variant displays