Map4k5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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57 records found for search term Map4k5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401736269	CV2689300	single nucleotide variant	NM_006575.6(MAP4K5):c.11C>G (p.Pro4Arg)	not specified [RCV004306132]	uncertain significance	14	50532039	50532039	Human		name
598197722	CV3985225	single nucleotide variant	NM_006575.6(MAP4K5):c.20C>T (p.Pro7Leu)	not specified [RCV005375461]	uncertain significance	14	50532030	50532030	Human		name
156248462	CV2357143	single nucleotide variant	NM_006575.6(MAP4K5):c.31A>G (p.Ile11Val)	not specified [RCV004206935]	uncertain significance	14	50532019	50532019	Human		name
156326895	CV2217163	single nucleotide variant	NM_006575.6(MAP4K5):c.104A>G (p.Tyr35Cys)	not specified [RCV004087622]	uncertain significance	14	50531946	50531946	Human		name
156236121	CV2245487	single nucleotide variant	NM_006575.6(MAP4K5):c.110C>T (p.Ala37Val)	not specified [RCV004109264]	uncertain significance	14	50504856	50504856	Human		name
405811474	CV3284959	single nucleotide variant	NM_006575.6(MAP4K5):c.125C>T (p.Thr42Ile)	not specified [RCV004408495]	uncertain significance	14	50504841	50504841	Human		name
405811478	CV3284961	single nucleotide variant	NM_006575.6(MAP4K5):c.187C>G (p.Gln63Glu)	not specified [RCV004408497]	uncertain significance	14	50486174	50486174	Human		name
405811480	CV3284962	single nucleotide variant	NM_006575.6(MAP4K5):c.189A>T (p.Gln63His)	not specified [RCV004408498]	uncertain significance	14	50486172	50486172	Human		name
597627702	CV3700300	single nucleotide variant	NM_006575.6(MAP4K5):c.273G>C (p.Trp91Cys)	not specified [RCV004938996]	uncertain significance	14	50485627	50485627	Human		name
598197746	CV3985228	single nucleotide variant	NM_006575.6(MAP4K5):c.259C>T (p.Arg87Trp)	not specified [RCV005375464]	uncertain significance	14	50485641	50485641	Human		name
15135315	CV714144	single nucleotide variant	NM_006575.6(MAP4K5):c.2193A>G (p.Val731=)	not provided [RCV000965268]	benign	14	50429232	50429232	Human		name
156158456	CV2236100	single nucleotide variant	NM_006575.6(MAP4K5):c.952C>T (p.Arg318Cys)	not specified [RCV004114250]	uncertain significance	14	50456579	50456579	Human		name
401861846	CV2766436	single nucleotide variant	NM_006575.6(MAP4K5):c.625A>G (p.Ile209Val)	not specified [RCV004345278]	uncertain significance	14	50468700	50468700	Human		name
401872532	CV2779704	single nucleotide variant	NM_006575.6(MAP4K5):c.458A>G (p.Asp153Gly)	not specified [RCV004351393]	uncertain significance	14	50476139	50476139	Human		name
401894272	CV2780560	single nucleotide variant	NM_006575.6(MAP4K5):c.658G>T (p.Asp220Tyr)	not specified [RCV004351936]	uncertain significance	14	50468667	50468667	Human		name
405811484	CV3284964	single nucleotide variant	NM_006575.6(MAP4K5):c.799A>C (p.Thr267Pro)	not specified [RCV004408500]	uncertain significance	14	50464072	50464072	Human		name
405811486	CV3284965	single nucleotide variant	NM_006575.6(MAP4K5):c.805G>C (p.Glu269Gln)	not specified [RCV004408501]	uncertain significance	14	50464066	50464066	Human		name
405811488	CV3284966	single nucleotide variant	NM_006575.6(MAP4K5):c.946A>G (p.Ile316Val)	not specified [RCV004408502]	uncertain significance	14	50456585	50456585	Human		name
598197731	CV3985226	single nucleotide variant	NM_006575.6(MAP4K5):c.832G>A (p.Ala278Thr)	not specified [RCV005375462]	uncertain significance	14	50462769	50462769	Human		name
598176314	CV3985234	single nucleotide variant	NM_006575.6(MAP4K5):c.953G>A (p.Arg318His)	not specified [RCV005371392]	uncertain significance	14	50456578	50456578	Human		name
598197790	CV3985235	single nucleotide variant	NM_006575.6(MAP4K5):c.524T>G (p.Phe175Cys)	not specified [RCV005375469]	uncertain significance	14	50475095	50475095	Human		name
598176320	CV3985236	single nucleotide variant	NM_006575.6(MAP4K5):c.766A>G (p.Ile256Val)	not specified [RCV005371393]	uncertain significance	14	50464105	50464105	Human		name
156028110	CV2195696	single nucleotide variant	NM_006575.6(MAP4K5):c.2435G>A (p.Arg812His)	not specified [RCV004076057]	uncertain significance	14	50423139	50423139	Human		name
156317760	CV2204053	single nucleotide variant	NM_006575.6(MAP4K5):c.1216T>C (p.Phe406Leu)	not specified [RCV004076523]	likely benign	14	50445164	50445164	Human		name
156283711	CV2231032	single nucleotide variant	NM_006575.6(MAP4K5):c.1713A>C (p.Lys571Asn)	not specified [RCV004094267]	uncertain significance	14	50438004	50438004	Human		name
156033592	CV2256462	single nucleotide variant	NM_006575.6(MAP4K5):c.1273G>A (p.Ala425Thr)	not specified [RCV004118674]	uncertain significance	14	50445107	50445107	Human		name
156092301	CV2256661	single nucleotide variant	NM_006575.6(MAP4K5):c.1303C>G (p.Pro435Ala)	not specified [RCV004118843]	uncertain significance	14	50445077	50445077	Human		name
155903148	CV2274828	single nucleotide variant	NM_006575.6(MAP4K5):c.1545G>T (p.Trp515Cys)	not specified [RCV004139165]	uncertain significance	14	50442751	50442751	Human		name
155928791	CV2281250	single nucleotide variant	NM_006575.6(MAP4K5):c.2215G>A (p.Val739Ile)	not provided [RCV004695498]\|not specified [RCV004147497]	uncertain significance	14	50429210	50429210	Human		name
156051975	CV2320266	single nucleotide variant	NM_006575.6(MAP4K5):c.2461G>A (p.Val821Ile)	not specified [RCV004178435]	uncertain significance	14	50420099	50420099	Human		name
156328785	CV2332312	single nucleotide variant	NM_006575.6(MAP4K5):c.1793C>G (p.Thr598Ser)	not specified [RCV004182482]	uncertain significance	14	50437924	50437924	Human		name
156168304	CV2337286	single nucleotide variant	NM_006575.6(MAP4K5):c.2491A>G (p.Thr831Ala)	not specified [RCV004187740]	uncertain significance	14	50420069	50420069	Human		name
156051533	CV2391250	single nucleotide variant	NM_006575.6(MAP4K5):c.2312G>A (p.Arg771His)	not specified [RCV004237261]	uncertain significance	14	50428676	50428676	Human		name
329352302	CV2452327	single nucleotide variant	NM_006575.6(MAP4K5):c.2288C>T (p.Ala763Val)	not specified [RCV004272660]	uncertain significance	14	50428700	50428700	Human		name
401737440	CV2699818	single nucleotide variant	NM_006575.6(MAP4K5):c.1156C>T (p.Arg386Cys)	not specified [RCV004308466]	uncertain significance	14	50446108	50446108	Human		name
401737585	CV2699854	single nucleotide variant	NM_006575.6(MAP4K5):c.1987C>G (p.His663Asp)	not specified [RCV004308496]	uncertain significance	14	50434571	50434571	Human		name
401776064	CV2706868	single nucleotide variant	NM_006575.6(MAP4K5):c.1390G>A (p.Ala464Thr)	not specified [RCV004321494]	uncertain significance	14	50443986	50443986	Human		name
401777189	CV2730178	single nucleotide variant	NM_006575.6(MAP4K5):c.1655G>A (p.Arg552Gln)	not specified [RCV004332455]	uncertain significance	14	50440063	50440063	Human		name
401902004	CV2810411	single nucleotide variant	NM_006575.6(MAP4K5):c.1354A>G (p.Ile452Val)	not provided [RCV003393422]	uncertain significance	14	50444022	50444022	Human		name
405811476	CV3284960	single nucleotide variant	NM_006575.6(MAP4K5):c.1831G>A (p.Ala611Thr)	not specified [RCV004408496]	uncertain significance	14	50437527	50437527	Human		name
405811482	CV3284963	single nucleotide variant	NM_006575.6(MAP4K5):c.2161G>A (p.Ala721Thr)	not specified [RCV004408499]	uncertain significance	14	50434397	50434397	Human		name
407494175	CV3446607	single nucleotide variant	NM_006575.6(MAP4K5):c.2159G>A (p.Gly720Asp)	not specified [RCV004642930]	uncertain significance	14	50434399	50434399	Human		name
407494179	CV3446608	single nucleotide variant	NM_006575.6(MAP4K5):c.2498A>G (p.His833Arg)	not specified [RCV004642931]	uncertain significance	14	50420062	50420062	Human		name
407494183	CV3446610	single nucleotide variant	NM_006575.6(MAP4K5):c.1087G>C (p.Asp363His)	not specified [RCV004642932]	uncertain significance	14	50447469	50447469	Human		name
597627672	CV3700294	single nucleotide variant	NM_006575.6(MAP4K5):c.1267A>G (p.Ser423Gly)	not specified [RCV004938990]	uncertain significance	14	50445113	50445113	Human		name
597627677	CV3700295	single nucleotide variant	NM_006575.6(MAP4K5):c.1255C>A (p.Pro419Thr)	not specified [RCV004938991]	uncertain significance	14	50445125	50445125	Human		name
597627680	CV3700296	single nucleotide variant	NM_006575.6(MAP4K5):c.1079T>C (p.Leu360Ser)	not specified [RCV004938992]	uncertain significance	14	50447477	50447477	Human		name
597627686	CV3700297	single nucleotide variant	NM_006575.6(MAP4K5):c.2061G>C (p.Met687Ile)	not specified [RCV004938993]	uncertain significance	14	50434497	50434497	Human		name
597627690	CV3700298	single nucleotide variant	NM_006575.6(MAP4K5):c.1105C>A (p.Gln369Lys)	not specified [RCV004938994]	uncertain significance	14	50447451	50447451	Human		name
597627696	CV3700299	single nucleotide variant	NM_006575.6(MAP4K5):c.1714A>C (p.Thr572Pro)	not specified [RCV004938995]	uncertain significance	14	50438003	50438003	Human		name
597627706	CV3700301	single nucleotide variant	NM_006575.6(MAP4K5):c.1451A>G (p.Asn484Ser)	not specified [RCV004938997]	uncertain significance	14	50443757	50443757	Human		name
598197738	CV3985227	single nucleotide variant	NM_006575.6(MAP4K5):c.1225G>A (p.Glu409Lys)	not specified [RCV005375463]	uncertain significance	14	50445155	50445155	Human		name
598197761	CV3985230	single nucleotide variant	NM_006575.6(MAP4K5):c.1427G>A (p.Arg476Gln)	not specified [RCV005375466]	uncertain significance	14	50443949	50443949	Human		name
598176307	CV3985231	single nucleotide variant	NM_006575.6(MAP4K5):c.1797C>G (p.His599Gln)	not specified [RCV005371391]	uncertain significance	14	50437920	50437920	Human		name
598197770	CV3985232	single nucleotide variant	NM_006575.6(MAP4K5):c.1147A>C (p.Thr383Pro)	not specified [RCV005375467]	uncertain significance	14	50446117	50446117	Human		name
598197779	CV3985233	single nucleotide variant	NM_006575.6(MAP4K5):c.2332C>A (p.Leu778Ile)	not specified [RCV005375468]	uncertain significance	14	50425972	50425972	Human		name
598197800	CV3985237	single nucleotide variant	NM_006575.6(MAP4K5):c.1198A>G (p.Ser400Gly)	not specified [RCV005375470]	uncertain significance	14	50445182	50445182	Human		name

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