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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRMT8, THCAT155
(A17T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRMT8
(P24R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(P34L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(N160D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(V167M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(V214M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(V244M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(T285M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(R291C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(A306T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
PRMT8
(R340Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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