Klf4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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61 records found for search term Klf4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405265280	CV3198445	single nucleotide variant	NM_004235.6(KLF4):c.1100-7C>A	KLF4-related disorder [RCV003897296]	benign	9	107487199	107487199	Human		name , trait , alternate_id
405267320	CV3202203	single nucleotide variant	NM_004235.6(KLF4):c.456T>C (p.Tyr152=)	KLF4-related disorder [RCV003911672]	likely benign	9	107487938	107487938	Human		name , trait , alternate_id
405279557	CV3206925	single nucleotide variant	NM_004235.6(KLF4):c.489G>T (p.Ala163=)	KLF4-related disorder [RCV003919483]	benign	9	107487905	107487905	Human		name , trait , alternate_id
405287551	CV3210691	single nucleotide variant	NM_004235.6(KLF4):c.504C>T (p.Gly168=)	KLF4-related disorder [RCV003924453]	benign	9	107487890	107487890	Human		name , trait , alternate_id
405291970	CV3221189	single nucleotide variant	NM_004235.6(KLF4):c.306C>G (p.Leu102=)	KLF4-related disorder [RCV003964279]	likely benign	9	107488088	107488088	Human		name , trait , alternate_id
407470216	CV3448433	single nucleotide variant	NM_004235.6(KLF4):c.47T>C (p.Leu16Pro)	not specified [RCV004637054]	uncertain significance	9	107489009	107489009	Human		name
597639074	CV3692156	single nucleotide variant	NM_004235.6(KLF4):c.49C>T (p.Leu17Phe)	not specified [RCV004941308]	uncertain significance	9	107489007	107489007	Human		name
15145972	CV736803	single nucleotide variant	NM_004235.6(KLF4):c.973C>T (p.Leu325=)	KLF4-related disorder [RCV003950549]\|not provided [RCV000900245]	benign\|likely benign	9	107487421	107487421	Human		name , trait , alternate_id
15191264	CV736804	single nucleotide variant	NM_004235.6(KLF4):c.691C>T (p.Leu231=)	not provided [RCV000910195]	likely benign	9	107487703	107487703	Human		name
156127526	CV2234719	single nucleotide variant	NM_004235.6(KLF4):c.253G>A (p.Gly85Ser)	not specified [RCV004102663]	uncertain significance	9	107488141	107488141	Human		name
156160496	CV2323367	single nucleotide variant	NM_004235.6(KLF4):c.208G>T (p.Val70Leu)	not specified [RCV004171768]	uncertain significance	9	107488186	107488186	Human		name
156337481	CV2343058	single nucleotide variant	NM_004235.6(KLF4):c.259A>G (p.Asn87Asp)	not specified [RCV004192655]	uncertain significance	9	107488135	107488135	Human		name
329399310	CV2436217	single nucleotide variant	NM_004235.6(KLF4):c.208G>A (p.Val70Met)	not specified [RCV004249846]	uncertain significance	9	107488186	107488186	Human		name
405268555	CV3219582	single nucleotide variant	NM_004235.6(KLF4):c.1179C>T (p.Thr393=)	KLF4-related disorder [RCV003969788]	likely benign	9	107487113	107487113	Human		name , trait , alternate_id
405807573	CV3265574	single nucleotide variant	NM_004235.6(KLF4):c.262C>A (p.Leu88Met)	not specified [RCV004406645]	uncertain significance	9	107488132	107488132	Human		name
597768543	CV3692151	single nucleotide variant	NM_004235.6(KLF4):c.188A>G (p.Tyr63Cys)	not specified [RCV004927510]	uncertain significance	9	107488206	107488206	Human		name
598220948	CV3976642	single nucleotide variant	NM_004235.6(KLF4):c.151A>T (p.Met51Leu)	not specified [RCV005360740]	uncertain significance	9	107488243	107488243	Human		name
15134367	CV711683	single nucleotide variant	NM_004235.6(KLF4):c.1404G>A (p.Ser468=)	KLF4-related disorder [RCV003905890]\|not provided [RCV000965113]	benign\|likely benign	9	107485787	107485787	Human		name , trait , alternate_id
15138442	CV711684	single nucleotide variant	NM_004235.6(KLF4):c.1113C>T (p.Pro371=)	KLF4-related disorder [RCV003943145]\|not provided [RCV000965792]	benign\|likely benign	9	107487179	107487179	Human		name , trait , alternate_id
15110242	CV723241	single nucleotide variant	NM_004235.6(KLF4):c.1158A>G (p.Arg386=)	KLF4-related disorder [RCV003930858]\|not provided [RCV000894022]	benign	9	107487134	107487134	Human		name , trait , alternate_id
15142548	CV736805	single nucleotide variant	NM_004235.6(KLF4):c.122A>G (p.Asn41Ser)	KLF4-related disorder [RCV003940837]\|not provided [RCV000899691]	likely benign	9	107488934	107488934	Human		name , trait , alternate_id
15157724	CV751295	single nucleotide variant	NM_004235.6(KLF4):c.1059C>G (p.Pro353=)	not provided [RCV000924921]	likely benign	9	107487335	107487335	Human		name
156100118	CV2306595	single nucleotide variant	NM_004235.6(KLF4):c.884G>A (p.Ser295Asn)	not specified [RCV004157198]	uncertain significance	9	107487510	107487510	Human		name
155963403	CV2308271	single nucleotide variant	NM_004235.6(KLF4):c.616C>T (p.Pro206Ser)	not specified [RCV004164766]	uncertain significance	9	107487778	107487778	Human		name
156053528	CV2361060	single nucleotide variant	NM_004235.6(KLF4):c.779C>G (p.Pro260Arg)	not specified [RCV004216256]	uncertain significance	9	107487615	107487615	Human		name
156386094	CV2364651	single nucleotide variant	NM_004235.6(KLF4):c.346C>T (p.Pro116Ser)	not specified [RCV004219541]	uncertain significance	9	107488048	107488048	Human		name
156098491	CV2370782	single nucleotide variant	NM_004235.6(KLF4):c.577G>C (p.Val193Leu)	not specified [RCV004209179]	uncertain significance	9	107487817	107487817	Human		name
329370300	CV2435539	single nucleotide variant	NM_004235.6(KLF4):c.872G>T (p.Gly291Val)	not specified [RCV004253177]	uncertain significance	9	107487522	107487522	Human		name
329380285	CV2444302	single nucleotide variant	NM_004235.6(KLF4):c.715G>A (p.Gly239Ser)	not specified [RCV004263064]	uncertain significance	9	107487679	107487679	Human		name
329402340	CV2454159	single nucleotide variant	NM_004235.6(KLF4):c.767A>G (p.Asp256Gly)	not specified [RCV004265651]	uncertain significance	9	107487627	107487627	Human		name
401776347	CV2692680	single nucleotide variant	NM_004235.6(KLF4):c.404C>T (p.Ser135Leu)	not specified [RCV004312399]	uncertain significance	9	107487990	107487990	Human		name
401771682	CV2693316	single nucleotide variant	NM_004235.6(KLF4):c.494G>C (p.Gly165Ala)	not specified [RCV004295279]	uncertain significance	9	107487900	107487900	Human		name
401751988	CV2723080	single nucleotide variant	NM_004235.6(KLF4):c.970G>T (p.Val324Leu)	not specified [RCV004327557]	likely benign	9	107487424	107487424	Human		name
401743607	CV2726127	single nucleotide variant	NM_004235.6(KLF4):c.779C>T (p.Pro260Leu)	not specified [RCV004326613]	uncertain significance	9	107487615	107487615	Human		name
401862626	CV2775313	single nucleotide variant	NM_004235.6(KLF4):c.350C>T (p.Pro117Leu)	not specified [RCV004348428]	uncertain significance	9	107488044	107488044	Human		name
401899246	CV2783774	single nucleotide variant	NM_004235.6(KLF4):c.491C>T (p.Pro164Leu)	not specified [RCV004360688]	uncertain significance	9	107487903	107487903	Human		name
401932423	CV2797408	single nucleotide variant	NM_004235.6(KLF4):c.341C>A (p.Thr114Asn)	KLF4-related disorder [RCV003408681]	uncertain significance	9	107488053	107488053	Human		name , trait , alternate_id
405256259	CV3203565	single nucleotide variant	NM_004235.6(KLF4):c.859C>T (p.His287Tyr)	KLF4-related disorder [RCV003939807]\|not provided [RCV005242511]	likely benign	9	107487535	107487535	Human		name , trait , alternate_id
405807575	CV3265575	single nucleotide variant	NM_004235.6(KLF4):c.430G>C (p.Ala144Pro)	not specified [RCV004406646]	uncertain significance	9	107487964	107487964	Human		name
405807577	CV3265576	single nucleotide variant	NM_004235.6(KLF4):c.431C>T (p.Ala144Val)	not specified [RCV004406647]	uncertain significance	9	107487963	107487963	Human		name
405807579	CV3265577	single nucleotide variant	NM_004235.6(KLF4):c.518A>G (p.Tyr173Cys)	not specified [RCV004406648]	uncertain significance	9	107487876	107487876	Human		name
405807581	CV3265578	single nucleotide variant	NM_004235.6(KLF4):c.682A>C (p.Lys228Gln)	not specified [RCV004406649]	uncertain significance	9	107487712	107487712	Human		name
405807583	CV3265579	single nucleotide variant	NM_004235.6(KLF4):c.821G>A (p.Cys274Tyr)	not specified [RCV004406650]	uncertain significance	9	107487573	107487573	Human		name
405807585	CV3265580	single nucleotide variant	NM_004235.6(KLF4):c.901G>C (p.Ala301Pro)	not specified [RCV004406651]	likely benign	9	107487493	107487493	Human		name
407470224	CV3448435	single nucleotide variant	NM_004235.6(KLF4):c.349C>G (p.Pro117Ala)	not specified [RCV004637056]	uncertain significance	9	107488045	107488045	Human		name
597639057	CV3692152	single nucleotide variant	NM_004235.6(KLF4):c.458C>A (p.Pro153Gln)	not specified [RCV004941305]	uncertain significance	9	107487936	107487936	Human		name
597639068	CV3692155	single nucleotide variant	NM_004235.6(KLF4):c.391T>G (p.Ser131Ala)	not specified [RCV004941307]	uncertain significance	9	107488003	107488003	Human		name
597768552	CV3692158	single nucleotide variant	NM_004235.6(KLF4):c.776A>G (p.His259Arg)	not specified [RCV004927512]	uncertain significance	9	107487618	107487618	Human		name
598182410	CV3976637	single nucleotide variant	NM_004235.6(KLF4):c.373T>C (p.Ser125Pro)	not specified [RCV005352730]	uncertain significance	9	107488021	107488021	Human		name
598161144	CV3976638	single nucleotide variant	NM_004235.6(KLF4):c.747C>A (p.Ser249Arg)	not specified [RCV005368378]	uncertain significance	9	107487647	107487647	Human		name
598161151	CV3976639	single nucleotide variant	NM_004235.6(KLF4):c.818C>T (p.Thr273Met)	not specified [RCV005368379]	likely benign	9	107487576	107487576	Human		name
598182417	CV3976640	single nucleotide variant	NM_004235.6(KLF4):c.995C>T (p.Pro332Leu)	not specified [RCV005352731]	uncertain significance	9	107487399	107487399	Human		name
598161156	CV3976641	single nucleotide variant	NM_004235.6(KLF4):c.937A>G (p.Ser313Gly)	not specified [RCV005368380]	uncertain significance	9	107487457	107487457	Human		name
156035855	CV2243411	single nucleotide variant	NM_004235.6(KLF4):c.1115G>C (p.Gly372Ala)	not specified [RCV004112385]	uncertain significance	9	107487177	107487177	Human		name
156389358	CV2373774	single nucleotide variant	NM_004235.6(KLF4):c.1085C>G (p.Pro362Arg)	not specified [RCV004224717]	uncertain significance	9	107487309	107487309	Human		name
405259599	CV3195116	single nucleotide variant	NM_004235.6(KLF4):c.1189A>T (p.Thr397Ser)	KLF4-related disorder [RCV003894313]	uncertain significance	9	107487103	107487103	Human		name , trait , alternate_id
405807571	CV3265573	single nucleotide variant	NM_004235.6(KLF4):c.1123A>G (p.Met375Val)	not specified [RCV004406644]	uncertain significance	9	107487169	107487169	Human		name
407470220	CV3448434	single nucleotide variant	NM_004235.6(KLF4):c.1054C>G (p.Leu352Val)	not specified [RCV004637055]	uncertain significance	9	107487340	107487340	Human		name
597768548	CV3692153	single nucleotide variant	NM_004235.6(KLF4):c.1009C>G (p.Pro337Ala)	not specified [RCV004927511]	uncertain significance	9	107487385	107487385	Human		name
597639062	CV3692154	single nucleotide variant	NM_004235.6(KLF4):c.1015G>A (p.Gly339Ser)	not specified [RCV004941306]	uncertain significance	9	107487379	107487379	Human		name
15190350	CV700718	deletion	NM_004235.6(KLF4):c.716_766del (p.Gly239_Pro255del)	KLF4-related disorder [RCV003935832]\|not provided [RCV000954448]	likely benign	9	107487628	107487678	Human		name , trait , alternate_id

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