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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFDN
(I526T +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(E617G +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(R951H +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(P1113A +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(K1155E +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(D1128E +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(M1296T +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(M1421V +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(D1492A +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
AFDN
(R1584L +6 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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