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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QTNF6
(D259N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(R234C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(M229V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(E225K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(A197T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(S180N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(R169H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(G162S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(E147G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(L163P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(E139K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(A118T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(R113K +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
C1QTNF6
(Y110F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(I71V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(D45E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(G36S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(M24V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(M38I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF6
(R7C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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