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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TMEM106A
(S6Y)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
TMEM106A
(S34C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
TMEM106A
(R117P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
TMEM106A
(F145S +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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