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Items: 70

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAFB
(P319S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(R307T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(S304A)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MAFB
(A302V)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MAFB
(K297M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MAFB
(V296I)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MAFB
(R289H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(R289C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(A288V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GUncertain significance
MAFB
(E278D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(G250C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
Multicentric carpo-tarsal osteolysis with or without nephropathy
+1 more
GBenign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GBenign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(S206N)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MAFB
(G205S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(G203S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MAFB
(H193Y)
Single nucleotide variant
(missense variant)
Duane retraction syndrome 3 with or without deafness
+3 more
GUncertain significance
MAFB
(G189R)
Single nucleotide variant
(missense variant)
MAFB-related disorder
+2 more
GConflicting classifications of pathogenicity
MAFB
(Q181L)
Single nucleotide variant
(missense variant)
Multicentric carpo-tarsal osteolysis with or without nephropathy
+2 more
GBenign/Likely benign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(A176T)
Single nucleotide variant
(missense variant)
Multicentric carpo-tarsal osteolysis with or without nephropathy
+2 more
GUncertain significance
MAFB
(P171S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(H165Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(D153H)
Single nucleotide variant
(missense variant)
Multicentric carpo-tarsal osteolysis with or without nephropathy
+2 more
GUncertain significance
MAFB
(V150M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MAFB
(P146A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(H135Q)
Single nucleotide variant
(missense variant)
Duane retraction syndrome 3 with or without deafness
+2 more
GUncertain significance
MAFB
(H134Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(H132Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(H131Q)
Single nucleotide variant
(missense variant)
Duane retraction syndrome 3 with or without deafness
+3 more
GConflicting classifications of pathogenicity
MAFB
(A130V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
MAFB
(R128L)
Single nucleotide variant
(missense variant)
not provided
GBenign
MAFB
(S123T)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(S114P)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(E98D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
MAFB
(P97S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(L85M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
MAFB
(T76N)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MAFB
(S69L)
Single nucleotide variant
(missense variant)
not provided
GPathogenic/Likely pathogenic
MAFB
(S65I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MAFB
(P63L)
Single nucleotide variant
(missense variant)
MAFB-related disorder
+1 more
GPathogenic
MAFB
(P63S)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(T58I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(S57Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
(S54L)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(P42L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
MAFB
(R41S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(D30A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
(E19Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GBenign/Likely benign
MAFB
(M7V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
MAFB
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MAFB
Deletion
not provided
GPathogenic
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