Annotation Detail

Information
Associated Genes
TSC2
Associated Variants
TSC2 p.Pro1675Leu (p.P1675L) ( ENST00000439673.6, ENST00000401874.7, ENST00000219476.9, ENST00000382538.10, ENST00000568454.6, ENST00000350773.9, ENST00000642206.2, ENST00000642365.2, ENST00000642561.1, ENST00000642797.1, ENST00000642936.1, ENST00000643088.1, ENST00000643946.1, ENST00000644043.1, ENST00000644329.1, ENST00000644335.1, ENST00000645186.2, ENST00000646388.1 )
TSC2 p.Pro1675Leu (p.P1675L) ( 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.5024C>T (p.Pro1675Leu) AND Tuberous sclerosis 2
ClinVar Allele ID
27432
ClinVar RefSeq Alternation Syntax
NM_001318831.2:c.4292C>T
ClinVar RefSeq Alternation Syntax
NM_000548.5:c.5024C>T
ClinVar RefSeq Alternation Syntax
NM_001370404.1:c.4892C>T
ClinVar RefSeq Alternation Syntax
NM_001363528.2:c.4826C>T
ClinVar RefSeq Alternation Syntax
NM_001318827.2:c.4715C>T
ClinVar RefSeq Alternation Syntax
NM_001318829.2:c.4679C>T
ClinVar RefSeq Alternation Syntax
NM_001318832.2:c.4856C>T
ClinVar RefSeq Alternation Syntax
NM_021055.3:c.4895C>T
ClinVar RefSeq Alternation Syntax
NM_001077183.3:c.4823C>T
ClinVar RefSeq Alternation Syntax
NM_001114382.3:c.4955C>T
ClinVar RefSeq Alternation Syntax
NM_001370405.1:c.4895C>T
Clinical Significance Description
Conflicting interpretations of pathogenicity
Clinical Significance Last Update
2024-04-04
Clinical Significance Review Status
criteria provided, conflicting interpretations
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000013201
ClinVar Disease
Tuberous sclerosis 2
Observed Origin Sample
germline
Pubmed
9302281
Drugs