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Items: 39

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INKA2
(H269R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(E283G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(P264L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(T276I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(T276P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(G251R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(P248S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(S237N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R236W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(S225T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(P220L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(V233L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(G216V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R219Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R201G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(I195M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R187H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R187C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(Q198R +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
INKA2
(R188H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R135Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R148W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(M146K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(R135Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(S112N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(T122R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(T107A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(S86N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(T89I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(A71T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(E60K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(P55L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(E53K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(G46V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2
(L30F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INKA2, LOC129931193
(E18D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INKA2, LOC129931193
(K16R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INKA2, LOC129931193
(K16E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INKA2
(T2M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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