Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 1:17371320 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5502, 2009_August_001_245_SDHB_185470_0008

This variation has 11 HGVS names - click the plus to show

1:g.17371320G>C
ENST00000475506.1:n.53C>G
ENST00000491274.1:n.143C>G
ENST00000485515.1:n.124C>G
ENST00000375499.3:c.136C>G
ENSP00000364649.3:p.Arg46Gly
ENST00000466613.1:n.148C>G
ENST00000463045.1:n.298C>G
LRG_316:g.14346C>G
LRG_316t1.1:c.136C>G
LRG_316p1.1:p.Arg46Gly

Variation displays