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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130061638, NT5C
(R47S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(F44S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(E39K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(P37S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(R28C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(G25D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(R24W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(G21D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(V7L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC130061638, NT5C
(A2V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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