Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance

Synonyms

LSDB 5502, 2009_August_001_245_SDHB_185470_0008

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

1:g.17044825G>C
ENST00000475506.1:n.53C>G
ENST00000491274.3:c.94C>G
ENSP00000480482.1:p.Arg32Gly
ENST00000485515.3:n.124C>G
ENST00000375499.5:c.136C>G
ENSP00000364649.3:p.Arg46Gly
ENST00000466613.2:n.148C>G
ENST00000463045.2:c.-36C>G
LRG_316:g.14346C>G
LRG_316t1.1:c.136C>G
LRG_316p1.1:p.Arg46Gly

Variation displays