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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DCTN1
Single nucleotide variant
(intron variant)
not specified
+4 more
GBenign
DCTN1
(R1049Q +6 more)
Single nucleotide variant
(missense variant +1 more)
Neuronopathy, distal hereditary motor, type 7B
+5 more
GBenign/Likely benign
DCTN1
Single nucleotide variant
(synonymous variant +1 more)
Neuronopathy, distal hereditary motor, type 7B
+4 more
GBenign/Likely benign
DCTN1
(R361Q +6 more)
Single nucleotide variant
(missense variant +1 more)
Neuronopathy, distal hereditary motor, type 7B
+5 more
GConflicting classifications of pathogenicity
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