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Items: 1 to 100 of 2412

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+2 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+2 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
not specified
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Lynch syndrome
+4 more
GBenign/Likely benign
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(splice donor variant +2 more)
MSH6-related disorder
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(5 prime UTR variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
(R3Q)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(Q4*)
Single nucleotide variant
(nonsense +1 more)
Hereditary cancer-predisposing syndrome
+8 more
GPathogenic/Likely pathogenic
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
(S5N)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(T6P)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
+2 more
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
+2 more
GLikely benign
MSH6
(L7M)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+5 more
GUncertain significance
MSH6
Single nucleotide variant
(5 prime UTR variant +3 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GLikely benign
MSH6
(Y8N)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
(S9G)
Single nucleotide variant
(missense variant +1 more)
Endometrial carcinoma
+5 more
GConflicting classifications of pathogenicity
MSH6
(F10L)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
(F11L)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+4 more
GConflicting classifications of pathogenicity
MSH6
(P12T)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+6 more
GConflicting classifications of pathogenicity
MSH6
(P12R)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GLikely benign
MSH6
(K13Q)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+4 more
GUncertain significance
MSH6
(K13E)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH6
(K13R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MSH6
(K13T)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 5
+6 more
GUncertain significance
MSH6
(S14A)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
MSH6
(S14F)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GConflicting classifications of pathogenicity
MSH6
(P15A)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH6
(P15S)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not provided
+2 more
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
(S18R)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH6
(A20fs)
Duplication
(frameshift variant +1 more)
Endometrial carcinoma
+3 more
GPathogenic/Likely pathogenic
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
MSH6
(A20V)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
(N21D)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 5
+3 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GLikely benign
MSH6
(K22E)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
+3 more
GUncertain significance
MSH6
(A23P)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH6
(A23T)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GUncertain significance
MSH6
(A23V)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
not specified
+2 more
GLikely benign
MSH6
(S24L)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GUncertain significance
MSH6
(A25S)
Single nucleotide variant
(missense variant +1 more)
not specified
+9 more
GConflicting classifications of pathogenicity
MSH6
(A25G)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(A25V)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
(R26S)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GLikely benign
MSH6
(A27fs)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+5 more
GBenign/Likely benign
MSH6
(S28L)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH6
(R29G)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(R29C)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome 5
+4 more
GBenign/Likely benign
MSH6
(E30Q)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
MSH6
(E30K)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GLikely benign
MSH6
(G32C)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GConflicting classifications of pathogenicity
MSH6
(G32D)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GConflicting classifications of pathogenicity
MSH6
(R33S)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GUncertain significance
MSH6
(R33L)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GUncertain significance
MSH6
(R33P)
Single nucleotide variant
(missense variant +1 more)
not provided
+6 more
GConflicting classifications of pathogenicity
MSH6
(A34T)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
MSH6
(A34G)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GBenign/Likely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+4 more
GBenign/Likely benign
MSH6
(A35V)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+1 more
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GConflicting classifications of pathogenicity
MSH6
(A36V)
Single nucleotide variant
(missense variant +1 more)
Hereditary nonpolyposis colon cancer
+8 more
GConflicting classifications of pathogenicity
MSH6
(A40fs)
Deletion
(frameshift variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic
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