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Links from Gene

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MAP9, MAP9-AS1
(S378T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(A421T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9-AS1, MAP9
(H441R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(L381M)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(A319V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(S451N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(N357K)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9, MAP9-AS1
(R367T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9-AS1, MAP9
(S363P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MAP9-AS1, MAP9
(I424L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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