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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYTH3
(R393Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYTH3
(I290M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYTH3
(D180A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYTH3
(R155Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CYTH3
(H138Y)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(M72I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(V58L)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(T50A)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(K42R)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(K42Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(I35V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(R29Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CYTH3
(L25V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
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