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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRAPPC12
(R166S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TRAPPC12
(A214V)
Single nucleotide variant
(missense variant)
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
GUncertain significance
TRAPPC12
(R533G)
Single nucleotide variant
(missense variant)
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
GUncertain significance
TRAPPC12
Single nucleotide variant
(splice acceptor variant)
Early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome
GLikely pathogenic
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