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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP39A1
(V454I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(G281D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(C414R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(A310T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(F135S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(V306L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(H272L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
CYP39A1
(V107F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(A278V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(N93D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(C190S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(S161P +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CYP39A1
(L7W +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CYP39A1
(F175V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(L2V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYP39A1
(M153V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CYP39A1
(N110D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CYP39A1
(V101F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CYP39A1
(F67L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CYP39A1
(F43L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CYP39A1
(R27C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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