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Items: 11

  • The following term was not found in ClinVar: oenotheroides.
  • Showing results for Turbina oenotheroides. Your search for Turbina oenotheroides retrieved no results.
Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH6
(E807K +2 more)
Single nucleotide variant
(missense variant)
not specified
+7 more
GConflicting classifications of pathogenicity
MLH1
(G738E +8 more)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
ATM
(K482Q)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
ATM
(P1354T)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+5 more
GConflicting classifications of pathogenicity
BRCA2
(R1160K)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BRCA2
(D1699G)
Single nucleotide variant
(missense variant)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
BRCA2
(P2153L)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
BRCA1, LOC126862571
(N1355del +21 more)
Microsatellite
(inframe_deletion +2 more)
not specified
+5 more
GConflicting classifications of pathogenicity
CHEK2
(I416del +4 more)
Deletion
(inframe_deletion)
Hereditary cancer-predisposing syndrome
+3 more
GUncertain significance
CHEK2
Single nucleotide variant
(splice donor variant)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic/Likely pathogenic
CHEK2
(D162G +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+4 more
GConflicting classifications of pathogenicity
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