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Links from Gene

Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
OTUD6B
(L130V +2 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GUncertain significance
LOC130000726, OTUD6B
(L5F)
Single nucleotide variant
(5 prime UTR variant +1 more)
OTUD6B-related condition
GUncertain significance
LOC130000726, OTUD6B
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GLikely benign
LOC130000726, OTUD6B
(L15V)
Single nucleotide variant
(5 prime UTR variant +1 more)
OTUD6B-related condition
GUncertain significance
OTUD6B
(E134G +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GLikely pathogenic
LOC130000726, OTUD6B
(L9V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GUncertain significance
LOC130000726, OTUD6B
(E7*)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GPathogenic
OTUD6B
(A184T +1 more)
Single nucleotide variant
(missense variant)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GUncertain significance
OTUD6B
(K161* +1 more)
Single nucleotide variant
(nonsense)
Intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies
GLikely pathogenic
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