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Items: 30

  • The following term was not found in ClinVar: ipomoea.
  • Showing results for Ipomoea bouvetii. Your search for Ipomoea bouvetii retrieved no results.
Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH2
(T33P)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome 1
+7 more
GConflicting classifications of pathogenicity
MSH2
(Y43C)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
MSH2
(E198G +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH2
(R243Q +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
MSH2
(A305T +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GConflicting classifications of pathogenicity
MSH2
(P349A +1 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+7 more
GConflicting classifications of pathogenicity
MSH2
(A434P +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+1 more
GConflicting classifications of pathogenicity
MSH2
(G548C +1 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
MSH2
(N583S +1 more)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+8 more
GConflicting classifications of pathogenicity
MSH2
(L602P +1 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+2 more
GConflicting classifications of pathogenicity
MSH2
(N671Y +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome 1
+1 more
GLikely pathogenic
MSH2
(C697R +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GPathogenic
MSH2
(R711Q +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
+3 more
GUncertain significance
MLH1
(N38H)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
MLH1
(T116K +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+7 more
GConflicting classifications of pathogenicity
MLH1
(A160V +2 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MLH1
(V185G +2 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
MLH1
(G244V +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+3 more
GConflicting classifications of pathogenicity
MLH1
(H264Y +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+6 more
GUncertain significance
MLH1
(E319K +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary nonpolyposis colorectal neoplasms
+8 more
GConflicting classifications of pathogenicity
MLH1
(N338S +3 more)
Single nucleotide variant
(missense variant +2 more)
Hereditary cancer-predisposing syndrome
+9 more
GConflicting classifications of pathogenicity
MLH1
(G454R +5 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colon cancer
+8 more
GConflicting classifications of pathogenicity
MLH1
(R474G +5 more)
Single nucleotide variant
(missense variant)
Colorectal cancer, hereditary nonpolyposis, type 2
+4 more
GConflicting classifications of pathogenicity
MLH1
(R474W +5 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MLH1
(R474Q +5 more)
Single nucleotide variant
(missense variant)
not provided
+5 more
GConflicting classifications of pathogenicity
MLH1
(A539D +5 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MLH1
(L582F +5 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GConflicting classifications of pathogenicity
MLH1
(A681T +7 more)
Single nucleotide variant
(missense variant +1 more)
Lynch syndrome
GPathogenic
GCK
Single nucleotide variant
(intron variant)
not provided
+1 more
GLikely pathogenic
HNF1A
Single nucleotide variant
(intron variant)
Monogenic diabetes
GUncertain significance
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