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Links from MedGen

Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INTS11
(A212fs +4 more)
Duplication
(frameshift variant)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GLikely pathogenic
INTS11
(E126K +4 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GUncertain significance
INTS11
(R130C +4 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GUncertain significance
INTS11
(R23L +1 more)
Single nucleotide variant
(missense variant +2 more)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GPathogenic
INTS11
(G61S +2 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GPathogenic
INTS11
(V521M +4 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INTS11
(L144F +2 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GPathogenic
INTS11
(H420Y +4 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
GPathogenic
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