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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNM1L
(L169F +1 more)
Single nucleotide variant
(missense variant +1 more)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
GUncertain significance
DNM1L
(K53fs +2 more)
Duplication
(frameshift variant)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
+1 more
GPathogenic
DNM1L
(G350R +2 more)
Single nucleotide variant
(missense variant)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
GUncertain significance
DNM1L
(G362S +2 more)
Single nucleotide variant
(missense variant)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
+1 more
GPathogenic
DNM1L
(E379K +2 more)
Single nucleotide variant
(missense variant)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
GLikely pathogenic
DNM1L
(R403C +2 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic
DNM1L
(Y691C +7 more)
Single nucleotide variant
(missense variant)
Encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1
+2 more
GPathogenic/Likely pathogenic
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