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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BTD
(C13fs)
Indel
(frameshift variant)
not provided
+1 more
GPathogenic
BTD
(V42M)
Single nucleotide variant
(missense variant)
Biotinidase deficiency
GPathogenic/Likely pathogenic
BTD
(A151T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
BTD
(P167fs)
Deletion
(frameshift variant +1 more)
Biotinidase deficiency
GPathogenic
BTD
(N182I)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
GConflicting classifications of pathogenicity
BTD
(C225Y)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
+1 more
GPathogenic/Likely pathogenic
BTD
(S291fs)
Deletion
(frameshift variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
BTD
(H303R)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
BTD
(I344fs)
Duplication
(frameshift variant +1 more)
Biotinidase deficiency
GPathogenic
BTD
(N369fs)
Duplication
(frameshift variant +1 more)
Biotinidase deficiency
GPathogenic
BTD
(P372del)
Microsatellite
(intron variant)
Biotinidase deficiency
GUncertain significance
BTD
(V397I +1 more)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
GUncertain significance
BTD
(L402fs)
Duplication
(frameshift variant +1 more)
Biotinidase deficiency
GPathogenic
BTD
(C403R)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
BTD
(D424H)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
+2 more
GPathogenic/Likely pathogenic
BTD
(Y434C)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
BTD
(Q436H)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
+2 more
GPathogenic/Likely pathogenic
BTD
(P477S)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
+1 more
GPathogenic/Likely pathogenic
BTD
(E487K +1 more)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
GUncertain significance
BTD
(L515V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
BTD
(R518C)
Single nucleotide variant
(missense variant +1 more)
Biotinidase deficiency
+2 more
GPathogenic
BTD
(R518H)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic/Likely pathogenic
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