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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPTBN4
(E475K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
SPTBN4
(R631* +1 more)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness
GLikely pathogenic
SPTBN4
(Q1197*)
Single nucleotide variant
(nonsense)
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness
GPathogenic
SPTBN4
(V1977M)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, neuropathy, and deafness
GUncertain significance
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