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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLXNA3
(N564S)
Single nucleotide variant
(missense variant)
Autism
GUncertain significance
PLXNA3
(I1210F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PLXNA3
Indel
(inframe_indel)
PLXNA3-associated seizure disorder
GUncertain significance
PLXNA3
(R108C)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism
GUncertain significance
PLXNA3
(R1359C)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism
GUncertain significance
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