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Items: 34

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130007872, SMARCD1
(P37L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130007872, SMARCD1
(P44L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LOC130007872, SMARCD1
(M53T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
SMARCD1
(Q93R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(N122S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
Microsatellite
(intron variant)
not provided
GBenign
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GBenign
SMARCD1
(A152fs)
Duplication
(frameshift variant)
not provided
GUncertain significance
SMARCD1
(L151fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
SMARCD1
(Q159H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(R165Q)
Single nucleotide variant
(missense variant)
See cases
+1 more
GConflicting classifications of pathogenicity
SMARCD1
(I168T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(I184V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(T189I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(R214W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GBenign
SMARCD1
(D247G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SMARCD1
(L255V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GBenign
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GBenign
SMARCD1
(P293A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(R300S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(I323V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(R334Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
SMARCD1
Single nucleotide variant
(intron variant)
not provided
GBenign
SMARCD1
(R438W)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
SMARCD1
(P432S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(Y455H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(V458M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(R503* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
SMARCD1
(R100C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMARCD1
(D298Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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