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Items: 19

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
C1QTNF7
(K7N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
C1QTNF7
(S15R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(R26W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(P46A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(S51C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(P52S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(H55P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(R57H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(G75S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(K112I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(P127A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(G141E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(R140G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(I154V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(I166M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(I206T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(I218V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(A230T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
C1QTNF7
(Q240H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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