Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:112088971 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000208

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003002.1:c.274G>T, 2010_April_001_294_SDHD_602690_0004, 11371

This variation has 23 HGVS names - click the plus to show

11:g.112088971G>T
ENST00000528182.3:c.274G>T
ENSP00000435475.1:p.Asp92Tyr
ENST00000525987.3:n.279G>T
ENST00000534010.1:c.105G>T
ENSP00000433202.1:p.Asp36Tyr
ENST00000526592.3:c.274G>T
ENSP00000432005.1:p.Asp92Tyr
ENST00000532699.1:c.274G>T
ENSP00000456434.1:p.Asp92Tyr
ENST00000614349.2:c.274G>T
ENSP00000480666.1:p.Asp92Tyr
ENST00000375549.5:c.274G>T
ENSP00000364699.3:p.Asp92Tyr
ENST00000528021.3:c.274G>T
ENSP00000432465.1:p.Asp92Tyr
ENST00000525291.3:c.157G>T
ENSP00000436669.1:p.Asp53Tyr
ENST00000530923.3:c.264G>T
ENSP00000432946.1:p.Asp89Tyr
ENST00000531744.3:c.274G>T
ENSP00000456957.1:p.Asp92Tyr
ENST00000528048.3:c.169+998G>T

Variation displays