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Links from Gene

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SMC3
(N426fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
SMC3
(Q1035R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SMC3
(E398fs)
Duplication
(frameshift variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(R634C)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(D564E)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(T857A)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(H527R)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(R928Q)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
(E449fs)
Duplication
Cornelia de Lange syndrome 3
GLikely pathogenic
SMC3
(I3V)
Single nucleotide variant
(missense variant)
Cornelia de Lange syndrome 3
GUncertain significance
SMC3
Deletion
(inframe_deletion)
not provided
GUncertain significance
SMC3
Deletion
(intron variant)
not specified
GLikely benign
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