Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 11:112088971 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM000208

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003002.1:c.274G>T, 2010_April_001_294_SDHD_602690_0004, 11371

HGVS names

This variant has 23 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, is associated with 4 phenotypes and is mentioned in 3 citations.

Variant displays