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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MINPP1
(L27fs)
Deletion
(frameshift variant)
Pontocerebellar hypoplasia, type 16
GLikely pathogenic
MINPP1
(A284D +1 more)
Single nucleotide variant
(missense variant +1 more)
Pontocerebellar hypoplasia, type 16
GLikely pathogenic
MINPP1
(I331S +1 more)
Single nucleotide variant
(missense variant +1 more)
Pontocerebellar hypoplasia, type 16
GConflicting classifications of pathogenicity
LOC126860990, MINPP1
(R404* +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Pontocerebellar hypoplasia, type 16
GLikely pathogenic
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