Annotation Detail

Information
Associated Genes
TSC2
Associated Variants
TSC2 p.Arg1743Trp (p.R1743W) ( ENST00000645186.2, ENST00000568454.6, ENST00000643088.1, ENST00000642561.1, ENST00000644335.1, ENST00000642206.2, ENST00000643946.1, ENST00000439673.6, ENST00000646388.1, ENST00000642365.2, ENST00000350773.9, ENST00000642797.1, ENST00000382538.10, ENST00000219476.9, ENST00000642936.1, ENST00000401874.7, ENST00000644329.1, ENST00000644043.1 )
TSC2 p.Arg1743Trp (p.R1743W) ( ENST00000219476.9, ENST00000350773.9, ENST00000382538.10, ENST00000401874.7, ENST00000439673.6, ENST00000568454.6, ENST00000642206.2, ENST00000642365.2, ENST00000642561.1, ENST00000642797.1, ENST00000642936.1, ENST00000643088.1, ENST00000643946.1, ENST00000644043.1, ENST00000644329.1, ENST00000644335.1, ENST00000645186.2, ENST00000646388.1 )
Associated Disease
tuberous sclerosis 2
Source Database
ClinVar
Description
NM_000548.5(TSC2):c.5227C>T (p.Arg1743Trp) AND Tuberous sclerosis 2
ClinVar Allele ID
58633
ClinVar RefSeq Alternation Syntax
NM_001370405.1:c.5086C>T
ClinVar RefSeq Alternation Syntax
NM_021055.3:c.5098C>T
ClinVar RefSeq Alternation Syntax
NM_000548.5:c.5227C>T
ClinVar RefSeq Alternation Syntax
NM_001318831.2:c.4495C>T
ClinVar RefSeq Alternation Syntax
NM_001114382.3:c.5158C>T
ClinVar RefSeq Alternation Syntax
NM_001318827.2:c.4918C>T
ClinVar RefSeq Alternation Syntax
NM_001318829.2:c.4882C>T
ClinVar RefSeq Alternation Syntax
NM_001077183.3:c.5026C>T
ClinVar RefSeq Alternation Syntax
NM_001363528.2:c.5029C>T
ClinVar RefSeq Alternation Syntax
NM_001370404.1:c.5095C>T
ClinVar RefSeq Alternation Syntax
NM_001318832.2:c.5059C>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2024-01-09
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000201065
ClinVar Disease
Tuberous sclerosis 2
Observed Origin Sample
germline
Observed Origin Sample
de novo
Observed Origin Sample
unknown
Drugs