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Items: 1 to 100 of 156

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYOC, MYOCOS
+540 more
Copy number loss
See cases
GPathogenic
LOC129932082, LOC129932083
+561 more
Copy number loss
See cases
GPathogenic
ABL2, ACBD6
+513 more
Copy number gain
See cases
GPathogenic
ABL2, ACBD6
+347 more
Copy number loss
See cases
GPathogenic
MIR488, MR1
+456 more
Copy number loss
See cases
GPathogenic
LOC129932021, LOC129932022
+478 more
Copy number loss
See cases
GPathogenic
APOBEC4, ARPC5
+160 more
Copy number loss
See cases
GPathogenic
RNASEL
(G732R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(A730T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
RNASEL-related disorder
GBenign
RNASEL
(Q718K)
Single nucleotide variant
(missense variant)
Ovarian cancer
GBenign
RNASEL
Deletion
(splice donor variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R667Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(R651G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(S628N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(R608Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(D604N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
RNASEL
(L566F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(V531M)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(splice acceptor variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(I493V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(N490S)
Single nucleotide variant
(missense variant)
Ovarian cancer
GLikely pathogenic
RNASEL
(L477fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L477M)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E474D)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(Q473P)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V472fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V472fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(A471V)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(A471fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(K470T)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(F469fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(F469L)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(F469I)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(I468fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(I468fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S467fs)
Insertion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S466fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L465M)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(N463S)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R462fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R462Q)
Single nucleotide variant
(missense variant)
Hereditary cancer
GLikely benign
RNASEL
(F460fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E459V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(E457fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E456D)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(N455fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E454fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V453fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E451fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(H448fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L441fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E438*)
Duplication
(nonsense)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(C437fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(T435P)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V434fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V432fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L430S)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L430*)
Single nucleotide variant
(nonsense)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L430fs)
Insertion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(H429fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(H429fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R427fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S425fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E424Q)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S423fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S423fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(G422W)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(Y421fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(F420fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(T419K)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(T419fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(T419fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(V418fs)
Insertion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L417F)
Single nucleotide variant
(missense variant)
Ovarian cancer
GBenign
RNASEL
(L417fs)
Duplication
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L417fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L417fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S415G)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
not provided
GBenign
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(E413K)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R412G)
Single nucleotide variant
(missense variant)
RNASEL-related disorder
GLikely benign
RNASEL
(R412fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(S410R)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(L408fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(C407Y)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(C407fs)
Deletion
(frameshift variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(R403P)
Single nucleotide variant
(missense variant)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
Single nucleotide variant
(synonymous variant)
not provided
GBenign
RNASEL
(E388D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RNASEL
(E376del)
Deletion
(inframe_deletion)
Prostate cancer, hereditary, 1
GUncertain significance
RNASEL
(A372D)
Single nucleotide variant
(missense variant)
Ovarian cancer
GLikely pathogenic
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