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Items: 26

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130001603, CDKN2A
Microsatellite
(inframe_deletion +2 more)
not specified
+5 more
GConflicting classifications of pathogenicity
CDKN2A, LOC130001603
(A4V)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A, LOC130001603
(A4G)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
LOC130001603, CDKN2A
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
CDKN2A, LOC130001603
(E2Q)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
CDKN2A, LOC130001603
(M1R)
Single nucleotide variant
(missense variant +2 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A, LOC130001603
(M1K)
Single nucleotide variant
(missense variant +2 more)
not specified
+3 more
GUncertain significance
LOC130001603, CDKN2A
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GBenign/Likely benign
CDKN2A, LOC130001603
Deletion
(genic upstream transcript variant +1 more)
Melanoma and neural system tumor syndrome
+1 more
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
CDKN2A-related disorder
+4 more
GConflicting classifications of pathogenicity
LOC130001603, CDKN2A
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
LOC130001603, CDKN2A
Deletion
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
CDKN2A, LOC130001603
Single nucleotide variant
(intron variant)
not provided
+4 more
GBenign/Likely benign
CDKN2A, LOC130001603
Single nucleotide variant
(intron variant)
Melanoma-pancreatic cancer syndrome
+3 more
GConflicting classifications of pathogenicity
LOC130001603, CDKN2A
Single nucleotide variant
(intron variant)
not specified
+5 more
GConflicting classifications of pathogenicity
CDKN2A, LOC130001603
Single nucleotide variant
(genic upstream transcript variant +1 more)
Melanoma and neural system tumor syndrome
+7 more
GPathogenic
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