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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCAF4
(V894I +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCAF4
(L828P +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCAF4
(A627V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCAF4
(P199R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCAF4
(Y83* +1 more)
Single nucleotide variant
(nonsense)
Fliedner-Zweier syndrome
GLikely pathogenic
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