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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130067853, PPP6R2
(A904T +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067853, PPP6R2
(M905V +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067853, PPP6R2
(D948H +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067853, PPP6R2
(R922H)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GLikely benign
LOC130067853, PPP6R2
(E923G +8 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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