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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MED17
(R189*)
Single nucleotide variant
(nonsense)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
+1 more
GPathogenic/Likely pathogenic
MED17
(D244N)
Single nucleotide variant
(missense variant)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
GUncertain significance
MED17
(S254C)
Single nucleotide variant
(missense variant)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
+2 more
GConflicting classifications of pathogenicity
MED17
(W291R)
Single nucleotide variant
(missense variant)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
GUncertain significance
MED17
(Q533*)
Single nucleotide variant
(nonsense)
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
+1 more
GConflicting classifications of pathogenicity
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