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Items: 1 to 100 of 418

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMN2
Single nucleotide variant
(5 prime UTR variant)
not provided
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(D31G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(K50Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
FMN2-related disorder
GLikely benign
FMN2
(G59del)
Microsatellite
(inframe_deletion)
Intellectual disability, autosomal recessive 47
GBenign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(G55fs)
Deletion
(frameshift variant)
Intellectual disability, autosomal recessive 47
+1 more
GConflicting classifications of pathogenicity
FMN2
Single nucleotide variant
(synonymous variant)
FMN2-related disorder
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(S76T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(R94S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(L98V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(L121I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
FMN2
(S124L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
FMN2
(I183F)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
+1 more
GLikely pathogenic
FMN2
(Q192L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
FMN2
(A202T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Microsatellite
(inframe_insertion)
FMN2-related disorder
+1 more
GBenign/Likely benign
FMN2
(Q210R)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
+1 more
GUncertain significance
FMN2
Microsatellite
(inframe_insertion)
not provided
+1 more
GBenign
FMN2
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
FMN2
(P232A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
FMN2-related disorder
GLikely benign
FMN2
(G244A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(G248S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(L254M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(A260T)
Single nucleotide variant
(missense variant)
not provided
GBenign
FMN2
(T269S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FMN2
(S282R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(R288W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(Q292*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal recessive 47
GLikely pathogenic
FMN2
(P293S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(S295P)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
FMN2
(S295F)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
GUncertain significance
FMN2
(G298D)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
FMN2
(A304T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(S306G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(P318L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(D344N)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
FMN2
(T345M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(D346N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(D352Y)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(W366*)
Single nucleotide variant
(nonsense)
not provided
GLikely pathogenic
FMN2
(A367V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FMN2
(P368R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(D390E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(P392S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(P403L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FMN2
Duplication
(inframe_insertion)
Inborn genetic diseases
GUncertain significance
FMN2
(F408L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(T415I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FMN2
(K420E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(K420T)
Single nucleotide variant
(missense variant)
not specified
+3 more
GConflicting classifications of pathogenicity
FMN2
(T421N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
FMN2
(N430S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(L451Q)
Single nucleotide variant
(missense variant)
FMN2-related disorder
+2 more
GBenign/Likely benign
FMN2
(R453Q)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
FMN2
(A458T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
FMN2
(A460T)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(A464S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(A466fs)
Duplication
(frameshift variant)
Intellectual disability, autosomal recessive 47
GPathogenic
FMN2
(R470W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
FMN2
(A491V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(P494R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(L503M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(A508V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(G513R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(P517fs)
Deletion
(frameshift variant)
Intellectual disability, autosomal recessive 47
GPathogenic
FMN2
(A529T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
(D531Y)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal recessive 47
Gnot provided
FMN2
(N535K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
FMN2
(R540*)
Single nucleotide variant
(nonsense)
Intellectual disability, autosomal recessive 47
GPathogenic
FMN2
(T541M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
FMN2
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
FMN2
(G553R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FMN2
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination