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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PORCN
(Q28*)
Single nucleotide variant
(5 prime UTR variant +1 more)
Focal dermal hypoplasia
GPathogenic
TPM1
(I130V +2 more)
Single nucleotide variant
(missense variant)
Pulmonary atresia with intact ventricular septum
GLikely pathogenic
TPM1
(S229F +2 more)
Single nucleotide variant
(missense variant)
Atrial septal defect 1
GLikely pathogenic
TPM1
Single nucleotide variant
(splice donor variant)
Tetralogy of Fallot
GLikely pathogenic
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