U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 61

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAPSN
(R404C +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(R338Q +1 more)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+3 more
GConflicting classifications of pathogenicity
RAPSN
(G336R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(N394S +1 more)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(R376Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
RAPSN
(R376W +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(E313G +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(V356M +1 more)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+4 more
GUncertain significance
RAPSN
(R346W +1 more)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(E274K +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(E274Q +1 more)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(E310K)
Single nucleotide variant
(missense variant +1 more)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(D303E)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
RAPSN
(A301V)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
RAPSN
(G291D)
Single nucleotide variant
(missense variant +1 more)
Congenital myasthenic syndrome 11
+3 more
GConflicting classifications of pathogenicity
RAPSN
(A288V)
Single nucleotide variant
(missense variant +1 more)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(L283P)
Single nucleotide variant
(missense variant +1 more)
Global developmental delay
+5 more
GConflicting classifications of pathogenicity
RAPSN
(L283V)
Single nucleotide variant
(missense variant +1 more)
Fetal akinesia deformation sequence 2
+2 more
GUncertain significance
RAPSN
(S274R)
Single nucleotide variant
(missense variant +1 more)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(A272T)
Single nucleotide variant
(missense variant +1 more)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(D261N)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(R259H)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GConflicting classifications of pathogenicity
RAPSN
(A246V)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 2
+3 more
GPathogenic/Likely pathogenic
RAPSN
(A236T)
Single nucleotide variant
(missense variant)
Congenital Myasthenic Syndrome, Recessive
+3 more
GUncertain significance
RAPSN
(M233V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(E227*)
Single nucleotide variant
(nonsense)
Fetal akinesia deformation sequence 1
+2 more
GPathogenic/Likely pathogenic
RAPSN
(G223S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(R217H)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(W200C)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(N194S)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(V165M)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
RAPSN
Single nucleotide variant
(synonymous variant)
Fetal akinesia deformation sequence 1
+2 more
GConflicting classifications of pathogenicity
RAPSN
(R164H)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 2
+1 more
GConflicting classifications of pathogenicity
RAPSN
(M160T)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+3 more
GUncertain significance
RAPSN
(A159T)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(D158G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(A153S)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
RAPSN
(R151C)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(A149T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
RAPSN
(A142D)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+4 more
GConflicting classifications of pathogenicity
RAPSN
(G122R)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
RAPSN
(Q120H)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
RAPSN
(Y105C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(C97*)
Single nucleotide variant
(nonsense)
Fetal akinesia deformation sequence 1
+2 more
GPathogenic
RAPSN
(C97Y)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(E94K)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
RAPSN
(L89V)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(N88K)
Single nucleotide variant
(missense variant)
Myopathy
+7 more
GPathogenic/Likely pathogenic
RAPSN
(L82P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(D80N)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(D78N)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+2 more
GUncertain significance
RAPSN
(T72M)
Single nucleotide variant
(missense variant)
Congenital myasthenic syndrome 11
+3 more
GUncertain significance
RAPSN
(V68I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(A66T)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
RAPSN
(K60Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GUncertain significance
RAPSN
(Y59C)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
RAPSN
(G57R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
RAPSN
(G47D)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(V45M)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 2
+3 more
GPathogenic/Likely pathogenic
RAPSN
(N20I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
RAPSN
(E11D)
Single nucleotide variant
(missense variant)
Fetal akinesia deformation sequence 1
+2 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination