Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 1:17044882 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020965, CD041934

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5500, 2009_August_001_244_SDHB_185470_0006

This variation has 22 HGVS names - click the plus to show

Variant allele A
1:g.17044882G>A
ENST00000491274.3:c.37C>T
ENSP00000480482.1:p.Arg13Ter
ENST00000485515.3:n.67C>T
ENST00000375499.5:c.79C>T
ENSP00000364649.3:p.Arg27Ter
ENST00000463045.2:c.-93C>T
ENST00000466613.2:n.91C>T
LRG_316:g.14289C>T
LRG_316t1.1:c.79C>T
LRG_316p1.1:p.Arg27Ter

Variant allele C
1:g.17044882G>C
ENST00000491274.3:c.37C>G
ENSP00000480482.1:p.Arg13Gly
ENST00000485515.3:n.67C>G
ENST00000375499.5:c.79C>G
ENSP00000364649.3:p.Arg27Gly
ENST00000463045.2:c.-93C>G
ENST00000466613.2:n.91C>G
LRG_316:g.14289C>G
LRG_316t1.1:c.79C>G
LRG_316p1.1:p.Arg27Gly

Variation displays