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Items: 1 to 100 of 162

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GBenign
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
Single nucleotide variant
(5 prime UTR variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P4S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(G9R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
(G9V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(R15P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(G21A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(G22S)
Single nucleotide variant
(missense variant +1 more)
HTRA2-related disorder
+1 more
GUncertain significance
HTRA2
(G26E)
Single nucleotide variant
(missense variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
+2 more
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P33S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
(R36W)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
HTRA2
(R36Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(A37S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(L38P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(L39M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(S44C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
(R47fs)
Duplication
(frameshift variant +1 more)
not provided
GPathogenic
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P46S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(P46R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(R49P)
Single nucleotide variant
(missense variant +1 more)
3-methylglutaconic aciduria type 8
+1 more
GUncertain significance
HTRA2
(V50M)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(G53R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(S56N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(W58S)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(W58C)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(R60W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
HTRA2
(V63I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(E67G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(P68S)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(L72P)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GBenign/Likely benign
HTRA2
(S74F)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(P79T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(R80L)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
HTRA2
(A81T)
Single nucleotide variant
(missense variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
GUncertain significance
HTRA2
(Q82*)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
HTRA2
(T84I)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(A85V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(S99F)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(G100R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(T101A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(R102H)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(W106R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(A110G)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(G112C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
(A116fs)
Duplication
(frameshift variant +1 more)
not provided
GPathogenic/Likely pathogenic
HTRA2
(G114A)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(L121del)
Microsatellite
(inframe_deletion +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
+1 more
GLikely benign
HTRA2
(L120F)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(W122del)
Deletion
(inframe_deletion +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P128L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(P129L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(L132V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
(A141fs)
Duplication
(frameshift variant +1 more)
not provided
GPathogenic
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P139Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(A141S)
Single nucleotide variant
(missense variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
+2 more
GBenign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(P143A)
Single nucleotide variant
(missense variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
Grisk factor
HTRA2
(S145N)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
HTRA2
(S145R)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(D152N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(E155del)
Deletion
(inframe_deletion +1 more)
not provided
GUncertain significance
HTRA2
(E155D)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
+2 more
GBenign/Likely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
Parkinson disease 13, autosomal dominant, susceptibility to
+1 more
GLikely benign
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(F172V)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
HTRA2
(R175P)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(V177I)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
HTRA2
(R204L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
Display optionsSort by LocationDownload
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