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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TSPEAR
(R279C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KRTAP10-1, TSPEAR
(D159E)
Single nucleotide variant
(missense variant +1 more)
Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
GBenign
KRTAP10-1, TSPEAR
(D159Y)
Single nucleotide variant
(missense variant +1 more)
Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
GBenign
KRTAP10-3, TSPEAR
(T3A)
Single nucleotide variant
(missense variant +1 more)
Ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
GBenign
KRTAP10-7, TSPEAR
(Y62C)
Single nucleotide variant
(missense variant +1 more)
not specified
GBenign
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