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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMARCD3
(E431K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(G426S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(T251M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(G164S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(R155W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(M110T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(A98V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(P63L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(P49S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SMARCD3
(M38K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD3
(H24Y)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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