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Items: 1 to 100 of 324

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
CDKN2A-related disorder
+2 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
CDKN2A-related disorder
+2 more
GLikely benign
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GBenign/Likely benign
CDKN2A
Duplication
(no sequence alteration +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(3 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Familial melanoma
+2 more
GLikely benign
CDKN2A
(D105Y +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(D156N +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Familial melanoma
+2 more
GLikely benign
CDKN2A
(I154N +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(intron variant)
Familial melanoma
+2 more
GLikely benign
CDKN2A
Single nucleotide variant
(intron variant)
Familial melanoma
+2 more
GLikely benign
CDKN2A
Single nucleotide variant
(intron variant)
Familial melanoma
+1 more
GLikely benign
CDKN2A
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(intron variant)
not provided
+4 more
GPathogenic/Likely pathogenic
CDKN2A
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GLikely benign
CDKN2A
Single nucleotide variant
(intron variant)
Familial melanoma
+1 more
GLikely benign
CDKN2A
(D153Y +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+4 more
GPathogenic/Likely pathogenic
CDKN2A
(S152L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CDKN2A
(G150R +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Familial melanoma
+2 more
GLikely benign
CDKN2A
(A148V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
CDKN2A
(A148T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GBenign
CDKN2A
(D146G +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
Melanoma and neural system tumor syndrome
+1 more
GUncertain significance
CDKN2A
(D95V +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(I145T +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
CDKN2A
(R144P +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R144L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CDKN2A
(R144G +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R144C +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+5 more
GBenign/Likely benign
CDKN2A
(A143G +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CDKN2A
(A143T +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
CDKN2A
(H142R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CDKN2A
(N141D +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(S140R +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+2 more
GUncertain significance
CDKN2A
(G139D +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+3 more
GUncertain significance
CDKN2A
(G139R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
CDKN2A
(G139S +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R138G +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
CDKN2A
(T137fs +1 more)
Duplication
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
CDKN2A
(G136D +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(G136fs +1 more)
Deletion
(frameshift variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GBenign/Likely benign
CDKN2A
(G135V +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+2 more
GUncertain significance
CDKN2A
(G135E +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Familial melanoma
+1 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
CDKN2A
(A133T +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GLikely benign
CDKN2A
(A132V +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(R131C +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Familial melanoma
+1 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GBenign/Likely benign
CDKN2A
(R128Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R128W +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(A127V +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(A127P +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
CDKN2A
(A127S +1 more)
Single nucleotide variant
(missense variant +1 more)
Melanoma-pancreatic cancer syndrome
+6 more
GBenign/Likely benign
CDKN2A
(V126D +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GPathogenic
CDKN2A
(V126L +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(D74G +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(D125H +1 more)
Single nucleotide variant
(missense variant +1 more)
Melanoma-pancreatic cancer syndrome
+4 more
GConflicting classifications of pathogenicity
CDKN2A
(R124S +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A
(R124G +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R124C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+5 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GLikely benign
CDKN2A
(H123Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+4 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
CDKN2A
(G122V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+6 more
GConflicting classifications of pathogenicity
CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GBenign/Likely benign
CDKN2A
(L121V +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
CDKN2A
(E120fs +1 more)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
CDKN2A
(P114fs +2 more)
Deletion
(frameshift variant +1 more)
Familial melanoma
+1 more
GPathogenic/Likely pathogenic
CDKN2A
(A118T +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(G132S)
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CDKN2A
(P131L)
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
CDKN2A
(D116E +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(V115E +1 more)
Single nucleotide variant
(missense variant +2 more)
Familial melanoma
+3 more
GUncertain significance
CDKN2A
(V115G +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(R129L +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+4 more
GUncertain significance
CDKN2A
(R129G)
Single nucleotide variant
(synonymous variant +2 more)
not specified
+3 more
GConflicting classifications of pathogenicity
CDKN2A
(A128T)
Single nucleotide variant
(synonymous variant +2 more)
Familial melanoma
+2 more
GConflicting classifications of pathogenicity
CDKN2A
Duplication
(inframe_insertion +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic
CDKN2A
(R112H +1 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A
(R61C +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(P126R +2 more)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+2 more
GPathogenic/Likely pathogenic
CDKN2A
(G111S +2 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
CDKN2A
(G125R +2 more)
Single nucleotide variant
(nonsense +2 more)
Familial melanoma
+1 more
GPathogenic
CDKN2A
(L124V)
Single nucleotide variant
(synonymous variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
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