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Items: 27

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTEN
(L171V)
Single nucleotide variant
(5 prime UTR variant +1 more)
PTEN hamartoma tumor syndrome
GBenign
PTEN
Single nucleotide variant
(synonymous variant +1 more)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
Microsatellite
(intron variant)
PTEN hamartoma tumor syndrome
GBenign
PTEN
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
PTEN
(A79T +1 more)
Single nucleotide variant
(missense variant +1 more)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+1 more
GConflicting classifications of pathogenicity
PTEN
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
PTEN
(K183* +1 more)
Duplication
(nonsense +1 more)
Breast and/or ovarian cancer
GLikely pathogenic
PTEN
Single nucleotide variant
(synonymous variant +1 more)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+3 more
GConflicting classifications of pathogenicity
PTEN
Deletion
(intron variant)
PTEN hamartoma tumor syndrome
GBenign
PTEN
Microsatellite
(intron variant)
Breast and/or ovarian cancer
+2 more
GBenign/Likely benign
PTEN
Duplication
(intron variant)
PTEN hamartoma tumor syndrome
+4 more
GBenign/Likely benign
PTEN
Duplication
(intron variant)
Glioma susceptibility 2
+7 more
GBenign/Likely benign
PTEN
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+1 more
GBenign
PTEN
Deletion
(intron variant)
PTEN hamartoma tumor syndrome
+2 more
GConflicting classifications of pathogenicity
PTEN
Deletion
(intron variant)
not specified
+4 more
GBenign/Likely benign
PTEN
Deletion
(intron variant)
Breast and/or ovarian cancer
+2 more
GBenign/Likely benign
PTEN
Single nucleotide variant
(intron variant)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
PTEN
(I280V +2 more)
Single nucleotide variant
(missense variant)
PTEN hamartoma tumor syndrome
GUncertain significance
PTEN
(P281A +2 more)
Single nucleotide variant
(missense variant)
PTEN hamartoma tumor syndrome
GUncertain significance
PTEN
Single nucleotide variant
(synonymous variant)
not specified
+5 more
GBenign/Likely benign
PTEN
(V317I +2 more)
Single nucleotide variant
(missense variant)
PTEN hamartoma tumor syndrome
+2 more
GUncertain significance
PTEN
(P354Q +2 more)
Single nucleotide variant
(missense variant)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
Single nucleotide variant
(synonymous variant)
PTEN hamartoma tumor syndrome
GLikely benign
PTEN
Single nucleotide variant
(synonymous variant)
PTEN hamartoma tumor syndrome
+5 more
GBenign/Likely benign
PTEN
Deletion
(3 prime UTR variant)
PTEN hamartoma tumor syndrome
GUncertain significance
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