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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TES
(C37R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(L46F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(R80C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(N98D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(P107S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(P200S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(I241V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(G247D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(K286N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(V348M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(V345M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(R365W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
TES
(Y368C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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