"Ambry Genetics"[submitter] AND "KLF5"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2529022	NM_001730.5(KLF5):c.26G>A (p.Ser9Asn)	KLF5, LOC130009879 (S9N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398405	NM_001730.5(KLF5):c.55C>T (p.Pro19Ser)	KLF5 (P19S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347257	NM_001730.5(KLF5):c.121C>G (p.Arg41Gly)	KLF5 (R41G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253642	NM_001730.5(KLF5):c.121C>T (p.Arg41Cys)	KLF5 (R41C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115336	NM_001730.5(KLF5):c.138C>G (p.Phe46Leu)	KLF5 (F46L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115337	NM_001730.5(KLF5):c.166C>T (p.His56Tyr)	KLF5 (H56Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115338	NM_001730.5(KLF5):c.208C>T (p.Pro70Ser)	KLF5 (P70S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115339	NM_001730.5(KLF5):c.209C>T (p.Pro70Leu)	KLF5 (P70L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458959	NM_001730.5(KLF5):c.218C>T (p.Pro73Leu)	KLF5 (P73L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3115340	NM_001730.5(KLF5):c.260A>C (p.Gln87Pro)	KLF5 (Q87P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458399	NM_001730.5(KLF5):c.280A>C (p.Lys94Gln)	KLF5 (K94Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354561	NM_001730.5(KLF5):c.313A>G (p.Ile105Val)	KLF5 (I105V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242828	NM_001730.5(KLF5):c.364C>A (p.Gln122Lys)	KLF5 (Q122K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242829	NM_001730.5(KLF5):c.365A>C (p.Gln122Pro)	KLF5 (Q31P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115341	NM_001730.5(KLF5):c.377A>G (p.Asp126Gly)	KLF5 (D126G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303869	NM_001730.5(KLF5):c.553G>T (p.Ala185Ser)	KLF5 (A94S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115342	NM_001730.5(KLF5):c.614A>G (p.Asn205Ser)	KLF5 (N114S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231071	NM_001730.5(KLF5):c.614A>C (p.Asn205Thr)	KLF5 (N114T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263086	NM_001730.5(KLF5):c.655C>G (p.Leu219Val)	KLF5 (L128V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115343	NM_001730.5(KLF5):c.722G>C (p.Ser241Thr)	KLF5 (S150T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115344	NM_001730.5(KLF5):c.812C>T (p.Pro271Leu)	KLF5 (P180L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343239	NM_001730.5(KLF5):c.853A>G (p.Thr285Ala)	KLF5 (T194A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115345	NM_001730.5(KLF5):c.884A>C (p.Gln295Pro)	KLF5 (Q204P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379757	NM_001730.5(KLF5):c.1024A>G (p.Asn342Asp)	KLF5 (N251D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115335	NM_001730.5(KLF5):c.1239G>T (p.Arg413Ser)	KLF5 (R413S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324473	NM_001730.5(KLF5):c.1316A>G (p.Asn439Ser)	KLF5 (N439S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26