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Items: 60

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSC1, AK8
+11 more
Deletion
Tuberous sclerosis 1
GPathogenic
TSC1
Single nucleotide variant
(synonymous variant)
Tuberous sclerosis 1
+5 more
GBenign/Likely benign
TSC1
Microsatellite
(inframe_insertion)
not provided
+3 more
GBenign/Likely benign
TSC1
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
TSC1
(Q936* +3 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic/Likely pathogenic
TSC1
(T899S +3 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
TSC1
(N770fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(N840fs +3 more)
Duplication
(frameshift variant)
Tuberous sclerosis 1
+2 more
GPathogenic
TSC1
Single nucleotide variant
(splice acceptor variant)
Tuberous sclerosis syndrome
+1 more
GPathogenic/Likely pathogenic
TSC1
(L740fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(V733fs +3 more)
Insertion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(N716fs +3 more)
Deletion
(frameshift variant)
Lymphangiomyomatosis
+5 more
GPathogenic
TSC1
Deletion
(splice acceptor variant +1 more)
Tuberous sclerosis 1
GPathogenic
TSC1
Deletion
(splice acceptor variant +1 more)
Tuberous sclerosis 1
GPathogenic
TSC1
(R786* +3 more)
Single nucleotide variant
(nonsense)
not provided
+2 more
GPathogenic
TSC1
(Q783* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(L781fs +3 more)
Insertion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(Y761* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
+1 more
GPathogenic
TSC1
(Q748* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(Q743* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
+1 more
GPathogenic
TSC1
(Y704* +3 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
TSC1
(Q580* +3 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
TSC1
(R692Q +3 more)
Single nucleotide variant
(missense variant)
Lymphangiomyomatosis
+4 more
GConflicting classifications of pathogenicity
TSC1
(R692* +3 more)
Single nucleotide variant
(nonsense)
Lymphangiomyomatosis
+5 more
GPathogenic
TSC1
Single nucleotide variant
(splice donor variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(K545* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GLikely pathogenic
TSC1
(Q654* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
+2 more
GPathogenic
TSC1
(M646V +3 more)
Single nucleotide variant
(missense variant)
Isolated focal cortical dysplasia type II
+4 more
GBenign/Likely benign
TSC1
(T514fs +3 more)
Microsatellite
(frameshift variant)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
TSC1
(K509fs +3 more)
Microsatellite
(frameshift variant)
not provided
+1 more
GPathogenic
TSC1
(Y483* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(K587* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(L543P +3 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis 1
+1 more
GUncertain significance
TSC1
(S418fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(D389fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(R509* +3 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
+4 more
GPathogenic
TSC1
(P375fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(R500* +3 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
TSC1
Single nucleotide variant
(synonymous variant)
Tuberous sclerosis 1
+5 more
GBenign
TSC1
(T416fs +3 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(L209fs +2 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(Q328* +2 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic/Likely pathogenic
TSC1
(M322T +2 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GBenign
TSC1
(S289* +2 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(R245* +2 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
+3 more
GPathogenic/Likely pathogenic
TSC1
(R228* +2 more)
Single nucleotide variant
(nonsense)
Hereditary cancer-predisposing syndrome
+4 more
GPathogenic
TSC1
Single nucleotide variant
(splice acceptor variant +1 more)
Tuberous sclerosis 1
GPathogenic
TSC1
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
TSC1
(F216fs +2 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
Deletion
(nonsense)
Tuberous sclerosis syndrome
+2 more
GPathogenic
TSC1
(N161fs +2 more)
Deletion
(frameshift variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(Y144* +2 more)
Single nucleotide variant
(nonsense)
Tuberous sclerosis 1
GPathogenic
TSC1
(L191R +2 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis 1
GPathogenic
TSC1
(H181P +2 more)
Single nucleotide variant
(missense variant)
Tuberous sclerosis 1
GLikely pathogenic
TSC1
Single nucleotide variant
(splice acceptor variant)
Tuberous sclerosis 1
GPathogenic/Likely pathogenic
TSC1
Single nucleotide variant
(intron variant)
Tuberous sclerosis 1
GPathogenic
TSC1
Single nucleotide variant
(splice donor variant +1 more)
Tuberous sclerosis 1
GPathogenic/Likely pathogenic
TSC1
(D15N)
Single nucleotide variant
(missense variant +1 more)
Tuberous sclerosis 1
+3 more
GConflicting classifications of pathogenicity
TSC1
Single nucleotide variant
(intron variant)
Tuberous sclerosis 1
+1 more
GConflicting classifications of pathogenicity
TSC1
Single nucleotide variant
(5 prime UTR variant)
Isolated focal cortical dysplasia type II
+1 more
GUncertain significance
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