Annotation Detail

Information
Associated Genes
TSC2
Associated Variants
TSC2 p.Arg611Trp (p.R611W) ( ENST00000401874.7, ENST00000350773.9, ENST00000219476.9, ENST00000382538.10, ENST00000568454.6, ENST00000439673.6, ENST00000642206.2, ENST00000642365.2, ENST00000642561.1, ENST00000642797.1, ENST00000642936.1, ENST00000643088.1, ENST00000643946.1, ENST00000644043.1, ENST00000644329.1, ENST00000644335.1, ENST00000645186.2, ENST00000646388.1 )
TSC2 p.Arg611Trp (p.R611W) ( 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
Hereditary cancer-predisposing syndrome
Source Database
ClinVar
Description
NM_000548.5(TSC2):c.1831C>T (p.Arg611Trp) AND Hereditary cancer-predisposing syndrome
ClinVar Allele ID
58805
ClinVar RefSeq Alternation Syntax
NM_000548.5:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001318829.2:c.1684C>T
ClinVar RefSeq Alternation Syntax
NM_001318831.2:c.1231C>T
ClinVar RefSeq Alternation Syntax
NM_001370404.1:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001370405.1:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001114382.3:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001318832.2:c.1864C>T
ClinVar RefSeq Alternation Syntax
NM_021055.3:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001077183.3:c.1831C>T
ClinVar RefSeq Alternation Syntax
NM_001318827.2:c.1720C>T
ClinVar RefSeq Alternation Syntax
NM_001363528.2:c.1831C>T
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2019-07-01
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000491813
ClinVar Disease
Hereditary cancer-predisposing syndrome
Observed Origin Sample
germline
Drugs