Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 1:17028721 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020967

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5503, 2009_August_001_246_SDHB_185470_0009

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

1:g.17028721C>T
ENST00000475506.1:n.219G>A
ENST00000491274.3:c.260G>A
ENSP00000480482.1:p.Cys87Tyr
ENST00000485515.3:n.290G>A
ENST00000375499.5:c.302G>A
ENSP00000364649.3:p.Cys101Tyr
ENST00000463045.2:c.131G>A
ENSP00000481376.1:p.Cys44Tyr
LRG_316:g.30450G>A
LRG_316t1.1:c.302G>A
LRG_316p1.1:p.Cys101Tyr

Variation displays