Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 1:17044825 (forward strand) | View in location tab

Co-located

with COSMIC COSM677083 (G/A) ; HGMD-PUBLIC CM020966, CM030519

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5502, 2009_August_001_245_SDHB_185470_0008

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and is associated with 3 phenotypes.

Variant displays