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Links from Gene

Items: 36

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KPNA2
(N346T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(R13H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(T73I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(E66D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(T61A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(E499K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(V401M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(A176V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(A143V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(V195G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(T61I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(Y415F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(K123R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(P63L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(S54N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(I178V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
(A60T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KPNA2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KPNA2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
AANAT, AATK
+226 more
Copy number gain
not provided
GPathogenic
ABCA6, ABCA8
+79 more
Copy number gain
not provided
GPathogenic
ACE, AMZ2
+77 more
Copy number gain
not provided
GPathogenic
LLGL2, MAP2K6
+119 more
Copy number gain
not provided
GLikely pathogenic
AANAT, AATK
+222 more
Copy number gain
not provided
GPathogenic
ALOX12, ALOX12B
+1143 more
Copy number gain
See cases
GPathogenic
SPEM2, TBCD
+1143 more
Copy number gain
See cases
GPathogenic
AANAT, AATK
+458 more
Copy number gain
See cases
GPathogenic
ABCA10, ABCA5
+18 more
Copy number gain
See cases
GUncertain significance
AMZ2, ARSG
+62 more
Copy number loss
See cases
GPathogenic
AARSD1, AATF
+2032 more
Copy number gain
See cases
GPathogenic
KPNA2, LINC00674
+2 more
Copy number gain
See cases
GLikely benign
C17orf58, KPNA2
+4 more
Copy number loss
See cases
GLikely benign
C17orf58, KPNA2
+4 more
Copy number gain
See cases
GBenign
C17orf58, KPNA2
+4 more
Copy number gain
See cases
GBenign/Likely benign
ABCA10, ABCA5
+85 more
Copy number loss
See cases
GPathogenic
LOC126862582, LOC126862583
+1753 more
Copy number gain
See cases
GPathogenic
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