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Items: 21

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP5F1B
(H527R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(E525D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(P512H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(Q493H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(I460M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(E448D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(I360V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(L335P)
Single nucleotide variant
(missense variant)
Hypermetabolism due to Defect in Mitochondrial Coupling
GPathogenic
ATP5F1B
(I251T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(P165R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(I132V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(E105V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(P81L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(D76V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(A59T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(S51F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(Y46C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(P37A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(P28L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ATP5F1B
(S25P)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ATP5F1B
(L20H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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