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Items: 40

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(G39E)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant +2 more)
Lynch syndrome
GBenign
MSH6
(S144I)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant +2 more)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant +1 more)
Lynch syndrome
GBenign
MSH6
(E220D +1 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GLikely benign
MSH6
(R248G +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GBenign/Likely benign
MSH6
(V352I +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colon cancer
+5 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH6
(P408R +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GUncertain significance
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GBenign
MSH6
(S201C +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
(V509A +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GLikely benign
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH6
(V558fs +2 more)
Microsatellite
(frameshift variant)
Lynch syndrome
GPathogenic
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
MSH6
(V878A +2 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH6
(H918Y +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GUncertain significance
MSH6
(R766Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+4 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome 1
GBenign
MSH6
(F1088fs +2 more)
Duplication
(frameshift variant)
Lynch syndrome
GPathogenic
MSH6
(F974fs +1 more)
Deletion
(frameshift variant)
Lynch syndrome
GPathogenic
MSH6
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
MSH6
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH6
(Y1159* +2 more)
Single nucleotide variant
(nonsense)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GPathogenic/Likely pathogenic
MSH6
(R870fs +2 more)
Microsatellite
(frameshift variant)
Hereditary nonpolyposis colorectal neoplasms
+4 more
GPathogenic
MSH6
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign
MSH6
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
MSH6
Microsatellite
(intron variant)
Lynch syndrome
GBenign
MSH6
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH6
(L1003fs +2 more)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
MSH6
Microsatellite
(splice donor variant)
Lynch syndrome
GLikely benign
MSH6
(E1335A +2 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+6 more
GConflicting classifications of pathogenicity
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