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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TARDBP
Single nucleotide variant
(missense variant)
TARDBP-related condition
+4 more
GConflicting classifications of pathogenicity
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
TARDBP-related condition
+4 more
GConflicting classifications of pathogenicity
TARDBP
Single nucleotide variant
(missense variant)
Motor neuron disease
+3 more
GPathogenic/Likely pathogenic
TARDBP
(G294V)
Single nucleotide variant
(missense variant)
TARDBP-related frontotemporal dementia
+2 more
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
+1 more
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
+1 more
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
TARDBP
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
+2 more
GPathogenic/Likely pathogenic
TARDBP
(Y374*)
Duplication
(nonsense)
TARDBP-related condition
GUncertain significance
TARDBP
Single nucleotide variant
(missense variant)
TARDBP-related condition
+3 more
GPathogenic/Likely pathogenic
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
+2 more
GConflicting classifications of pathogenicity
TARDBP
Single nucleotide variant
(missense variant)
Amyotrophic lateral sclerosis type 10
Gnot provided
TARDBP
Single nucleotide variant
(3 prime UTR variant)
Amyotrophic lateral sclerosis type 10
Gnot provided
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