Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 11:112094906 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013285

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003002.1:c.416T>C, 2010_April_001_301_SDHD_602690_0016, 11383

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays