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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CDKN2A
Duplication
(inframe_insertion +1 more)
not provided
+3 more
GPathogenic
CDKN2A
(A109P +2 more)
Single nucleotide variant
(missense variant +1 more)
Melanoma-pancreatic cancer syndrome
+5 more
GUncertain significance
CDKN2A
(A51fs +2 more)
Insertion
(frameshift variant +1 more)
Familial melanoma
+1 more
GPathogenic/Likely pathogenic
CDKN2A
(R29P +1 more)
Single nucleotide variant
(missense variant +2 more)
Familial melanoma
+1 more
GUncertain significance
CDKN2A
(R24P)
Single nucleotide variant
(missense variant +1 more)
Melanoma and neural system tumor syndrome
+5 more
GPathogenic/Likely pathogenic
CDKN2A
(R22W)
Single nucleotide variant
(missense variant +1 more)
Familial melanoma
+3 more
GUncertain significance
CDKN2A
Microsatellite
(inframe_insertion +2 more)
Melanoma-pancreatic cancer syndrome
+5 more
GPathogenic/Likely pathogenic
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