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Items: 1 to 100 of 1638

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Breast and/or ovarian cancer
+2 more
GConflicting classifications of pathogenicity
MSH2
Duplication
(5 prime UTR variant)
Lynch syndrome 1
+2 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH2
Duplication
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+1 more
GUncertain significance
MSH2
Microsatellite
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(intron variant +1 more)
not provided
+2 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Lynch syndrome
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Lynch syndrome 1
+5 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Breast and/or ovarian cancer
+3 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
MSH2-related disorder
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
(M1V)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GUncertain significance
MSH2
(M1L)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GUncertain significance
MSH2
(M1T)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
(M1R)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
Duplication
(inframe_insertion +2 more)
not provided
+2 more
GUncertain significance
MSH2
(A2T)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
GLikely benign
MSH2
(A2E)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
(A2V)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+5 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not provided
+5 more
GLikely benign
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
GLikely benign
MSH2
(V3L)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GBenign
MSH2
(V3M)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GUncertain significance
MSH2
(Q4K)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
MSH2
(Q4P)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MSH2
(Q4L)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MSH2
(P5S)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH2
(P5R)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MSH2
(P5Q)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
+8 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+1 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GLikely benign
MSH2
(K6E)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
MSH2
(E7K)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
(E7*)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
GConflicting classifications of pathogenicity
MSH2
(E7A)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+4 more
GConflicting classifications of pathogenicity
MSH2
(E7G)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GLikely benign
MSH2
(T8R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MSH2
(T8M)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GBenign
MSH2
(L9M)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH2
(E12Q)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MSH2
(E12D)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH2
(S13N)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
+3 more
GConflicting classifications of pathogenicity
MSH2
(S13R)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+2 more
GUncertain significance
MSH2
(A14T)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome 1
+3 more
GBenign/Likely benign
MSH2
(A15V)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH2
(E16D)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH2
(V17I)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
MSH2
(F19L)
Single nucleotide variant
(missense variant +1 more)
not specified
+7 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH2
(V20M)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH2
(R21L)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
+2 more
GLikely benign
MSH2
(F22L)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GLikely benign
MSH2
(F23L)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
MSH2
(Q24E)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GConflicting classifications of pathogenicity
MSH2
(Q24*)
Single nucleotide variant
(nonsense +1 more)
Lynch syndrome 1
+5 more
GConflicting classifications of pathogenicity
MSH2
(Q24R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH2
(Q24H)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH2
(G25D)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
+5 more
GConflicting classifications of pathogenicity
MSH2
(P27T)
Single nucleotide variant
(missense variant +1 more)
not specified
+4 more
GConflicting classifications of pathogenicity
MSH2
(P27L)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colon cancer
+7 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
MSH2
(P30R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
(P30L)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
+4 more
GConflicting classifications of pathogenicity
MSH2
(T33fs)
Duplication
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
GPathogenic
MSH2
(T32S)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GLikely benign
MSH2
(T33A)
Single nucleotide variant
(missense variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
MSH2
(T33P)
Single nucleotide variant
(missense variant +1 more)
Muir-Torré syndrome
+7 more
GConflicting classifications of pathogenicity
MSH2
(T33I)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH2
(V34M)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MSH2
(R35G)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
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