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 11:112087916 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM000206

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11369, 2010_April_001_292_SDHD_602690_0002, NM_003002.1:c.112C>T

This variation has 21 HGVS names - click the plus to show

11:g.112087916C>T
ENST00000528182.3:c.112C>T
ENSP00000435475.1:p.Arg38Ter
ENST00000525987.3:n.117C>T
ENST00000526592.3:c.112C>T
ENSP00000432005.1:p.Arg38Ter
ENST00000614349.2:c.112C>T
ENSP00000480666.1:p.Arg38Ter
ENST00000532699.1:c.112C>T
ENSP00000456434.1:p.Arg38Ter
ENST00000375549.5:c.112C>T
ENSP00000364699.3:p.Arg38Ter
ENST00000528021.3:c.112C>T
ENSP00000432465.1:p.Arg38Ter
ENST00000525291.3:c.53-951C>T
ENST00000531744.3:c.112C>T
ENSP00000456957.1:p.Arg38Ter
ENST00000530923.3:c.102C>T
ENSP00000432946.1:p.Arg35Ter
ENST00000528048.3:c.112C>T
ENSP00000436217.1:p.Arg38Ter

Variation displays