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Items: 32

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APC
(M18K)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(R216* +3 more)
Single nucleotide variant
(nonsense +2 more)
Familial adenomatous polyposis 1
+8 more
GPathogenic
APC
(T256P +5 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(D364G +6 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
APC
(R405* +6 more)
Single nucleotide variant
(nonsense +1 more)
Familial adenomatous polyposis 1
+4 more
GPathogenic
APC
(R396S +10 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
Single nucleotide variant
(intron variant)
Classic or attenuated familial adenomatous polyposis
+9 more
GPathogenic/Likely pathogenic
APC
(Q462H +12 more)
Single nucleotide variant
(missense variant)
Classic or attenuated familial adenomatous polyposis
+4 more
GUncertain significance
APC
(M467I +12 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
APC
(R499* +12 more)
Single nucleotide variant
(nonsense)
Familial multiple polyposis syndrome
+3 more
GPathogenic
APC
(D381N +18 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
APC
(R402G +18 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
APC
(K408Q +18 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(R858* +12 more)
Single nucleotide variant
(nonsense)
Familial adenomatous polyposis 1
+3 more
GPathogenic
APC
(H753Y +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+1 more
GUncertain significance
APC
(K939R +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
APC
Deletion
(frameshift variant +1 more)
Familial multiple polyposis syndrome
+5 more
GPathogenic
APC
(S1126R +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+4 more
GConflicting classifications of pathogenicity
APC
(T1160K +12 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
APC
(E1056D +12 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
APC
(E1149fs +12 more)
Microsatellite
(frameshift variant)
Familial adenomatous polyposis 1
GPathogenic
APC
(R1676del +12 more)
Deletion
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
APC
(N1782S +12 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GUncertain significance
APC
(H1879P +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
APC
(M2195I +12 more)
Single nucleotide variant
(missense variant)
APC-Associated Polyposis Disorders
+8 more
GConflicting classifications of pathogenicity
APC
(S2207C +12 more)
Single nucleotide variant
(missense variant)
Classic or attenuated familial adenomatous polyposis
+4 more
GUncertain significance
APC
(N2022I +18 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
APC
(S2371fs +12 more)
Duplication
(frameshift variant)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic/Likely pathogenic
APC
(R2507C +12 more)
Single nucleotide variant
(missense variant)
Familial adenomatous polyposis 1
+5 more
GUncertain significance
APC
(V2612A +12 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
APC
(R2721H +12 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
APC
(I2756V +12 more)
Single nucleotide variant
(missense variant)
Ovarian cancer
+6 more
GConflicting classifications of pathogenicity
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