This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

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

Co-located

with HGMD-PUBLIC CD041934, CM020965

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5500, 2009_August_001_244_SDHB_185470_0006

This variation has 30 HGVS names - click the plus to show

Variant allele A
1:g.17044882G>A
ENST00000491274.4:c.37C>T
ENSP00000480482.1:p.Arg13Ter
ENST00000485515.4:n.67C>T
ENST00000375499.6:c.79C>T
ENSP00000364649.3:p.Arg27Ter
ENST00000463045.2:c.-93C>T
ENST00000466613.2:n.91C>T
LRG_316:g.14289C>T
LRG_316t1:c.79C>T
LRG_316p1:p.Arg27Ter

Variant allele T
1:g.17044882G>T
ENST00000491274.4:c.37C>A
ENST00000485515.4:n.67C>A
ENST00000375499.6:c.79C>A
ENST00000463045.2:c.-93C>A
ENST00000466613.2:n.91C>A
LRG_316:g.14289C>A
LRG_316t1:c.79C>A

Variant allele C
1:g.17044882G>C
ENST00000491274.4:c.37C>G
ENSP00000480482.1:p.Arg13Gly
ENST00000485515.4:n.67C>G
ENST00000375499.6:c.79C>G
ENSP00000364649.3:p.Arg27Gly
ENST00000463045.2:c.-93C>G
ENST00000466613.2:n.91C>G
LRG_316:g.14289C>G
LRG_316t1:c.79C>G
LRG_316p1:p.Arg27Gly

About this variant

This variant overlaps 21 transcripts and is associated with 6 phenotypes.

Variation displays