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Links from Gene

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MUSK
Deletion
Fetal akinesia deformation sequence 1
+1 more
GLikely pathogenic
MUSK
Deletion
Fetal akinesia deformation sequence 1
+1 more
GPathogenic
MUSK
Deletion
Fetal akinesia deformation sequence 1
+1 more
GPathogenic
MUSK
Deletion
Fetal akinesia deformation sequence 1
+1 more
GPathogenic
MUSK
(D198N +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(R168K +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(S386C +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
MUSK
(P138L +3 more)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
GUncertain significance
MUSK
(E90*)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
MUSK
(Y394C +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(A208T +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(F166C +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(W366R +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(R442G +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(S420R +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(S397F +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(Y331H +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
Single nucleotide variant
(intron variant)
Congenital myasthenic syndrome 9
+2 more
GConflicting classifications of pathogenicity
MUSK
(T85I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(F376L +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(I7T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(K337Q +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MUSK
(T780I +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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