SEPSECS Chromosome 4

Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
84 variants 84 Health Risk

Upload your DNA to see your personal genotypes for variants in SEPSECS.

What This Gene Does
The amino acid selenocysteine is the only amino acid that does not have its own tRNA synthetase. Instead, this amino acid is synthesized on its cognate tRNA in a three step process. The protein encoded by this gene catalyzes the third step in the process, the conversion of O-phosphoseryl-tRNA(Sec) to selenocysteinyl-tRNA(Sec).[provided by RefSeq, Mar 2011]
Associated Conditions (8)
Pontocerebellar hypoplasia type 2D
Pontoneocerebellar hypoplasia
SEPSECS-related disorder
Spastic ataxia
7 conditions
6 conditions
Inborn genetic diseases
Neurodevelopmental abnormality
Key Variants
RS146539065
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
Health Risk
RS1728415390
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS200041461
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS368514215
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS374407543
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, SEPSECS-related disorder, Pontocerebellar hypoplasia type 2D
Health Risk
RS587780457
Conflicting classifications of pathogenicity
Health Risk
RS61747281
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS747732980
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS757504141
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
RS773876739
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
Health Risk
RS773969315
Conflicting classifications of pathogenicity
Spastic ataxia, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
Health Risk
RS777854893
Conflicting classifications of pathogenicity
Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
Health Risk
All Variants (84)
RSID Category Clinical Significance Conditions
RS146539065 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
RS1728415390 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS200041461 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS368514215 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS374407543 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, SEPSECS-related disorder, Pontocerebellar hypoplasia type 2D
RS587780457 Health Risk Conflicting classifications of pathogenicity
RS61747281 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS747732980 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS757504141 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS773876739 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
RS773969315 Health Risk Conflicting classifications of pathogenicity Spastic ataxia, Pontoneocerebellar hypoplasia, Pontocerebellar hypoplasia type 2D
RS777854893 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS779387647 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS991789621 Health Risk Conflicting classifications of pathogenicity Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS1057518887 Health Risk Likely pathogenic 7 conditions, Pontocerebellar hypoplasia type 2D, 7 conditions
RS1204867394 Health Risk Likely pathogenic
RS1356750726 Health Risk Likely pathogenic
RS1430819064 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS1553878395 Health Risk Likely pathogenic 6 conditions, 6 conditions
RS1553881788 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1577599764 Health Risk Likely pathogenic
RS1577629146 Health Risk Likely pathogenic
RS2109021958 Health Risk Likely pathogenic
RS2109022340 Health Risk Likely pathogenic
RS2109029105 Health Risk Likely pathogenic
RS2109034260 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS2109035570 Health Risk Likely pathogenic
RS2109038924 Health Risk Likely pathogenic
RS2474659952 Health Risk Likely pathogenic
RS2474680639 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS754373273 Health Risk Likely pathogenic Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS1025711998 Health Risk Pathogenic Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D, Pontocerebellar hypoplasia type 2D
RS1030663609 Health Risk Pathogenic
RS1228958177 Health Risk Pathogenic
RS1260383512 Health Risk Pathogenic
RS1363933594 Health Risk Pathogenic
RS1367362454 Health Risk Pathogenic
RS1419508373 Health Risk Pathogenic
RS1471893777 Health Risk Pathogenic
RS1553881510 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1560336118 Health Risk Pathogenic
RS1560336134 Health Risk Pathogenic
RS1712331034 Health Risk Pathogenic
RS1712607979 Health Risk Pathogenic
RS1712612783 Health Risk Pathogenic
RS2109022156 Health Risk Pathogenic
RS2109022168 Health Risk Pathogenic
RS2109032673 Health Risk Pathogenic
RS2109032716 Health Risk Pathogenic
RS2109034059 Health Risk Pathogenic
Sign Up to Analyze Your DNA Log In