Original source

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

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

Chromosome 11:111959663 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD094779, CM000207

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11370, NM_003002.1:c.242C>T, 2010_April_001_293_SDHD_602690_0003

This variation has 22 HGVS names - click the plus to show

11:g.111959663C>T
ENST00000528182.1:c.242C>T
ENSP00000435475.1:p.Pro81Leu
ENST00000525987.1:n.247C>T
ENST00000534010.1:c.73C>T
ENSP00000433202.1:p.Pro25Leu
ENST00000526592.1:c.242C>T
ENSP00000432005.1:p.Pro81Leu
HG388_HG400_PATCH:g.111959662C>T
ENST00000532699.1:c.242C>T
ENSP00000456434.1:p.Pro81Leu
ENST00000375549.3:c.242C>T
ENSP00000364699.3:p.Pro81Leu
ENST00000528021.1:c.242C>T
ENSP00000432465.1:p.Pro81Leu
ENST00000525291.1:c.125C>T
ENSP00000436669.1:p.Pro42Leu
ENST00000530923.1:c.232C>T
ENSP00000432946.1:p.Pro78Leu
ENST00000531744.1:c.242C>T
ENSP00000456957.1:p.Pro81Leu
ENST00000528048.1:c.169+966C>T

Variation displays