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Links from MedGen

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1I
(S1008F +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GUncertain significance
CACNA1I
(E437del)
Microsatellite
(inframe_deletion)
Neurodevelopmental disorder with speech impairment and with or without seizures
GUncertain significance
CACNA1I
(G941R +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GUncertain significance
CACNA1I
(P285L)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GUncertain significance
CACNA1I
(R1131L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CACNA1I
(P1052L +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GUncertain significance
CACNA1I
(M1425I +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GPathogenic
CACNA1I
(I860M +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GPathogenic
CACNA1I
(I860N +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with speech impairment and with or without seizures
GPathogenic
CACNA1I
(I1306T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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