Original source

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

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

Chromosome 1:17371377 (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 20 HGVS names - click the plus to show

Variant allele A
1:g.17371377G>A
ENST00000491274.1:n.86C>T
ENST00000485515.1:n.67C>T
ENST00000375499.3:c.79C>T
ENSP00000364649.3:p.Arg27Ter
ENST00000466613.1:n.91C>T
ENST00000463045.1:n.241C>T
LRG_316:g.14289C>T
LRG_316t1.1:c.79C>T
LRG_316p1.1:p.Arg27Ter

Variant allele C
1:g.17371377G>C
ENST00000491274.1:n.86C>G
ENST00000485515.1:n.67C>G
ENST00000375499.3:c.79C>G
ENSP00000364649.3:p.Arg27Gly
ENST00000466613.1:n.91C>G
ENST00000463045.1:n.241C>G
LRG_316:g.14289C>G
LRG_316t1.1:c.79C>G
LRG_316p1.1:p.Arg27Gly

Variation displays