Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 11:112089002 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000209, CM094775

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_295_SDHD_602690_0005, 11372

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

11:g.112089002A>T
ENST00000528182.2:c.305A>T
ENSP00000435475.1:p.His102Leu
ENST00000525987.2:n.310A>T
ENST00000534010.1:c.136A>T
ENSP00000433202.1:p.His46Leu
ENST00000526592.2:c.305A>T
ENSP00000432005.1:p.His102Leu
ENST00000614349.1:c.305A>T
ENSP00000480666.1:p.His102Leu
ENST00000532699.1:c.305A>T
ENSP00000456434.1:p.His102Leu
ENST00000375549.4:c.305A>T
ENSP00000364699.3:p.His102Leu
ENST00000528021.2:c.305A>T
ENSP00000432465.1:p.His102Leu
ENST00000525291.2:c.188A>T
ENSP00000436669.1:p.His63Leu
ENST00000531744.2:c.305A>T
ENSP00000456957.1:p.His102Leu
ENST00000530923.2:c.295A>T
ENSP00000432946.1:p.His99Leu
ENST00000528048.2:c.169+1029A>T

Variation displays