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Items: 97

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
KLF11
Duplication
(intron variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(intron variant)
not provided
+1 more
GLikely benign
KLF11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
KLF11
(I17V)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
KLF11
(R29Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
KLF11
(E32K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(Q62R +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KLF11
Single nucleotide variant
(synonymous variant)
Maturity-onset diabetes of the young type 7
+1 more
GBenign/Likely benign
KLF11
(V64I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(T65N +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(P75A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(P92L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KLF11
Deletion
(intron variant)
not provided
GBenign
KLF11
(C88F +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(S101L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(T136M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(D137G +1 more)
Single nucleotide variant
(missense variant)
Monogenic diabetes
+2 more
GBenign/Likely benign
KLF11
(A126V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
KLF11
(A146V +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign/Likely benign
KLF11
(V146L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(A153T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(T156S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(V175M +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(E181K +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GLikely benign
KLF11
(S182R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
KLF11
(T192A +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(G203E +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(G203E +1 more)
Indel
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(Q198K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(T217I +1 more)
Single nucleotide variant
(missense variant)
KLF11-related disorder
+1 more
GUncertain significance
KLF11
(T220M +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
KLF11
(S225R +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(L243V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(P236R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(P261L +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign/Likely benign
KLF11
(E248K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(P264R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(P289T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(V314L +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(I300T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(L318R +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+2 more
GConflicting classifications of pathogenicity
KLF11
(G331V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(G329V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
(A330S +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+1 more
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KLF11
Single nucleotide variant
(synonymous variant)
Maturity-onset diabetes of the young type 7
+1 more
GLikely benign
KLF11
(A352T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(N340S +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
KLF11
(M359I +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(T360I +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+1 more
GConflicting classifications of pathogenicity
KLF11
(S379R +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
KLF11
(C365R +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GBenign
KLF11
Variation
(no sequence alteration)
not provided
GBenign
KLF11
(R402Q +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+2 more
GBenign/Likely benign
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
KLF11
Deletion
(splice acceptor variant)
not provided
+1 more
GUncertain significance
KLF11
(K433R +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(K417N +1 more)
Single nucleotide variant
(missense variant)
KLF11-related disorder
+1 more
GUncertain significance
KLF11
(F435Y +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+1 more
GConflicting classifications of pathogenicity
KLF11
(R437L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(K453del +1 more)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
KLF11
(R444Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
KLF11
(M464V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(S449C +1 more)
Single nucleotide variant
(missense variant)
Maturity-onset diabetes of the young type 7
+2 more
GUncertain significance
KLF11
(R457Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(M477V +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
KLF11
(P466S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
(P501L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KLF11
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
ADAM17, ASAP2
+10 more
Duplication
not provided
GUncertain significance
ADAM17, ASAP2
+10 more
Deletion
not provided
GPathogenic
KLF11
Duplication
not provided
GUncertain significance
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