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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSFM
(I107M)
Single nucleotide variant
(missense variant)
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
GUncertain significance
TSFM
(G108R)
Single nucleotide variant
(missense variant)
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
+1 more
GUncertain significance
TSFM
(E250* +1 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
GPathogenic
TSFM
(C315Y +1 more)
Single nucleotide variant
(3 prime UTR variant +2 more)
Fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3
+1 more
GLikely pathogenic
AVIL, TSFM
(N750K)
Single nucleotide variant
(missense variant +1 more)
Nephrotic syndrome, type 21
GUncertain significance
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