"Ambry Genetics"[submitter] AND "KLF11"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2555842	NM_003597.5(KLF11):c.20C>T (p.Ala7Val)	KLF11 (A7V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2168959	NM_003597.5(KLF11):c.49A>G (p.Ile17Val)	KLF11 (I17V)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2476421	NM_003597.5(KLF11):c.74T>C (p.Leu25Pro)	KLF11 (L25P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115267	NM_003597.5(KLF11):c.278A>G (p.Glu93Gly)	KLF11 (E76G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2321449	NM_003597.5(KLF11):c.350C>T (p.Pro117Leu)	KLF11 (P100L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489585	NM_003597.5(KLF11):c.412G>A (p.Val138Ile)	KLF11 (V138I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2327364	NM_003597.5(KLF11):c.422C>T (p.Ser141Phe)	KLF11 (S124F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1430360	NM_003597.5(KLF11):c.437C>T (p.Ala146Val)	KLF11 (A146V +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 2246492	NM_003597.5(KLF11):c.451G>C (p.Gly151Arg)	KLF11 (G134R +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375218	NM_003597.5(KLF11):c.458C>T (p.Ala153Val)	KLF11 (A153V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1930375	NM_003597.5(KLF11):c.523G>A (p.Val175Met)	KLF11 (V175M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3115268	NM_003597.5(KLF11):c.587G>A (p.Arg196Gln)	KLF11 (R179Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2315864	NM_003597.5(KLF11):c.630C>G (p.His210Gln)	KLF11 (H193Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331761	NM_003597.5(KLF11):c.655C>G (p.Leu219Val)	KLF11 (L202V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314968	NM_003597.5(KLF11):c.754T>C (p.Trp252Arg)	KLF11 (W235R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115269	NM_003597.5(KLF11):c.899C>T (p.Pro300Leu)	KLF11 (P300L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115270	NM_003597.5(KLF11):c.917C>T (p.Pro306Leu)	KLF11 (P289L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385335	NM_003597.5(KLF11):c.938C>T (p.Thr313Ile)	KLF11 (T296I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1923432	NM_003597.5(KLF11):c.940G>C (p.Val314Leu)	KLF11 (V314L +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3115263	NM_003597.5(KLF11):c.1117C>G (p.Pro373Ala)	KLF11 (P356A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115264	NM_003597.5(KLF11):c.1118C>T (p.Pro373Leu)	KLF11 (P356L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 330638	NM_003597.5(KLF11):c.1137C>G (p.Ser379Arg)	KLF11 (S379R +1 more)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 7 +2 more	GConflicting classifications of pathogenicity
Select item 2539746	NM_003597.5(KLF11):c.1144T>C (p.Cys382Arg)	KLF11 (C365R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3115265	NM_003597.5(KLF11):c.1249A>G (p.Thr417Ala)	KLF11 (T417A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456793	NM_003597.5(KLF11):c.1252C>T (p.His418Tyr)	KLF11 (H418Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396621	NM_003597.5(KLF11):c.1313C>T (p.Ser438Leu)	KLF11 (S438L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608578	NM_003597.5(KLF11):c.1348G>A (p.Gly450Arg)	KLF11 (G433R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115266	NM_003597.5(KLF11):c.1393C>T (p.Arg465Cys)	KLF11 (R465C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615096	NM_003597.5(KLF11):c.1457A>G (p.Gln486Arg)	KLF11 (Q469R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 892940	NM_003597.5(KLF11):c.1486G>A (p.Ala496Thr)	KLF11 (A496T +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2482561	NM_003597.5(KLF11):c.1504G>A (p.Gly502Arg)	KLF11 (G502R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 31