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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCTN1
Single nucleotide variant
(intron variant)
DCTN1-related condition
+6 more
GBenign/Likely benign
DCTN1
(P1084S +7 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+4 more
GUncertain significance
DCTN1
(R1049Q +6 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+6 more
GConflicting classifications of pathogenicity
DCTN1
(E737K +6 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+4 more
GUncertain significance
DCTN1
(L720V +6 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
DCTN1
Single nucleotide variant
(synonymous variant +1 more)
Amyotrophic lateral sclerosis type 1
+3 more
GConflicting classifications of pathogenicity
DCTN1
Single nucleotide variant
(synonymous variant +1 more)
Neuronopathy, distal hereditary motor, type 7B
+5 more
GBenign/Likely benign
DCTN1
(R532G +6 more)
Single nucleotide variant
(missense variant +1 more)
Amyotrophic lateral sclerosis type 1
+3 more
GUncertain significance
DCTN1
Single nucleotide variant
(intron variant +1 more)
DCTN1-Related Disorders
+6 more
GConflicting classifications of pathogenicity
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