Zpbp Variant Search Result - Rat Genome Database

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64 records found for search term Zpbp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405289973	CV3214043	single nucleotide variant	NM_007009.3(ZPBP):c.*1G>A	ZPBP-related disorder [RCV003926886]	likely benign	7	49937527	49937527	Human		name , trait , alternate_id
405284477	CV3196856	single nucleotide variant	NM_007009.3(ZPBP):c.784-7G>A	ZPBP-related disorder [RCV003979723]	benign	7	49983526	49983526	Human		name , trait , alternate_id
405256300	CV3203593	single nucleotide variant	NM_007009.3(ZPBP):c.208+4T>G	ZPBP-related disorder [RCV003939832]	likely benign	7	50089625	50089625	Human		name , trait , alternate_id
405291516	CV3205756	single nucleotide variant	NM_007009.3(ZPBP):c.208+4T>C	ZPBP-related disorder [RCV003963891]	likely benign	7	50089625	50089625	Human		name , trait , alternate_id
405274724	CV3209061	single nucleotide variant	NM_007009.3(ZPBP):c.488-9T>G	ZPBP-related disorder [RCV003951817]	likely benign	7	50031319	50031319	Human		name , trait , alternate_id
405295072	CV3210971	single nucleotide variant	NM_007009.3(ZPBP):c.707-7T>C	ZPBP-related disorder [RCV003936979]	benign	7	50018323	50018323	Human		name , trait , alternate_id
156082793	CV2244430	single nucleotide variant	NM_007009.3(ZPBP):c.77C>T (p.Ala26Val)	not specified [RCV004100399]	uncertain significance	7	50093118	50093118	Human		name
405265196	CV3195430	single nucleotide variant	NM_007009.3(ZPBP):c.43C>T (p.Arg15Trp)	ZPBP-related disorder [RCV003897321]	likely benign	7	50093152	50093152	Human		name , trait , alternate_id
405258378	CV3203675	single nucleotide variant	NM_007009.3(ZPBP):c.498G>A (p.Glu166=)	ZPBP-related disorder [RCV003941868]	likely benign	7	50031300	50031300	Human		name , trait , alternate_id
405276250	CV3206619	single nucleotide variant	NM_007009.3(ZPBP):c.375T>C (p.Leu125=)	ZPBP-related disorder [RCV003917062]	benign	7	50058101	50058101	Human		name , trait , alternate_id
405292930	CV3207042	single nucleotide variant	NM_007009.3(ZPBP):c.312G>A (p.Gly104=)	ZPBP-related disorder [RCV003931458]	likely benign	7	50081796	50081796	Human		name , trait , alternate_id
405256092	CV3208602	single nucleotide variant	NM_007009.3(ZPBP):c.74G>C (p.Arg25Pro)	ZPBP-related disorder [RCV003939675]	benign	7	50093121	50093121	Human		name , trait , alternate_id
598205059	CV3896777	deletion	NM_007009.3(ZPBP):c.116del (p.Val39fs)	Spermatogenic failure 66 [RCV005356958]	uncertain significance	7	50093079	50093079	Human	1	name
598276343	CV3942118	single nucleotide variant	NM_007009.3(ZPBP):c.37A>T (p.Arg13Trp)	not specified [RCV005305477]	likely benign	7	50093158	50093158	Human		name
15193443	CV700132	single nucleotide variant	NM_007009.3(ZPBP):c.50G>C (p.Arg17Pro)	ZPBP-related disorder [RCV003978280]\|not provided [RCV000955371]\|not specified [RCV001731992]	benign\|likely benign	7	50093145	50093145	Human	1	name , trait , alternate_id
156090556	CV2206617	single nucleotide variant	NM_007009.3(ZPBP):c.260C>T (p.Thr87Met)	not specified [RCV004080958]	uncertain significance	7	50081848	50081848	Human		name
156287161	CV2370465	single nucleotide variant	NM_007009.3(ZPBP):c.290A>C (p.Asp97Ala)	not specified [RCV004215814]	uncertain significance	7	50081818	50081818	Human		name
401783340	CV2716301	single nucleotide variant	NM_007009.3(ZPBP):c.288A>G (p.Ile96Met)	not specified [RCV004325301]	uncertain significance	7	50081820	50081820	Human		name
405675781	CV3354969	single nucleotide variant	NM_007009.3(ZPBP):c.143G>A (p.Arg48Gln)	not specified [RCV004487596]	uncertain significance	7	50089694	50089694	Human		name
407487528	CV3420966	single nucleotide variant	NM_007009.3(ZPBP):c.215C>T (p.Ala72Val)	not specified [RCV004603787]	likely benign	7	50081893	50081893	Human		name
407487546	CV3420969	single nucleotide variant	NM_007009.3(ZPBP):c.155C>G (p.Ala52Gly)	not specified [RCV004603790]	likely benign	7	50089682	50089682	Human		name
597747991	CV3646129	single nucleotide variant	NM_007009.3(ZPBP):c.223A>G (p.Met75Val)	not specified [RCV004892049]	uncertain significance	7	50081885	50081885	Human		name
598200527	CV3942117	single nucleotide variant	NM_007009.3(ZPBP):c.247G>A (p.Val83Met)	not specified [RCV005314073]	uncertain significance	7	50081861	50081861	Human		name
151757873	CV1336280	single nucleotide variant	NM_007009.3(ZPBP):c.931C>T (p.Gln311Ter)	Spermatogenic failure 66 [RCV001849239]	pathogenic	7	49983372	49983372	Human	1	name
156264257	CV2198557	single nucleotide variant	NM_007009.3(ZPBP):c.992G>A (p.Arg331His)	not specified [RCV004075583]	uncertain significance	7	49937592	49937592	Human		name
155925391	CV2348380	single nucleotide variant	NM_007009.3(ZPBP):c.344G>A (p.Arg115His)	not specified [RCV004193575]	uncertain significance	7	50058132	50058132	Human		name
156226286	CV2352729	single nucleotide variant	NM_007009.3(ZPBP):c.914G>T (p.Gly305Val)	not specified [RCV004198751]	uncertain significance	7	49983389	49983389	Human		name
329358275	CV2450247	single nucleotide variant	NM_007009.3(ZPBP):c.427G>A (p.Glu143Lys)	not specified [RCV004271351]	uncertain significance	7	50058049	50058049	Human		name
329397532	CV2456273	single nucleotide variant	NM_007009.3(ZPBP):c.995A>T (p.Asp332Val)	not specified [RCV004275447]	uncertain significance	7	49937589	49937589	Human		name
401724601	CV2738072	single nucleotide variant	NM_007009.3(ZPBP):c.557A>G (p.Tyr186Cys)	Spermatogenic failure 66 [RCV003315281]	uncertain significance	7	50031241	50031241	Human	1	name
405277408	CV3195496	single nucleotide variant	NM_007009.3(ZPBP):c.521C>G (p.Thr174Arg)	ZPBP-related disorder [RCV003904278]	benign	7	50031277	50031277	Human		name , trait , alternate_id
405675786	CV3354970	single nucleotide variant	NM_007009.3(ZPBP):c.902G>A (p.Arg301His)	not specified [RCV004487597]	uncertain significance	7	49983401	49983401	Human		name
407487534	CV3420967	single nucleotide variant	NM_007009.3(ZPBP):c.893G>C (p.Trp298Ser)	not specified [RCV004603788]	uncertain significance	7	49983410	49983410	Human		name
597747970	CV3646125	single nucleotide variant	NM_007009.3(ZPBP):c.832G>A (p.Gly278Ser)	not specified [RCV004892045]	uncertain significance	7	49983471	49983471	Human		name
597747975	CV3646126	single nucleotide variant	NM_007009.3(ZPBP):c.416C>T (p.Thr139Ile)	not specified [RCV004892046]	uncertain significance	7	50058060	50058060	Human		name
597747981	CV3646127	single nucleotide variant	NM_007009.3(ZPBP):c.653G>A (p.Arg218His)	not specified [RCV004892047]	likely benign	7	50031145	50031145	Human		name
597747986	CV3646128	single nucleotide variant	NM_007009.3(ZPBP):c.731G>T (p.Gly244Val)	not specified [RCV004892048]	uncertain significance	7	50018292	50018292	Human		name
597747997	CV3646130	single nucleotide variant	NM_007009.3(ZPBP):c.715C>G (p.Leu239Val)	not specified [RCV004892050]	uncertain significance	7	50018308	50018308	Human		name
598200533	CV3942119	single nucleotide variant	NM_007009.3(ZPBP):c.781A>G (p.Lys261Glu)	not specified [RCV005314074]	uncertain significance	7	50018242	50018242	Human		name
598190409	CV4008832	single nucleotide variant	NM_007009.3(ZPBP):c.739C>T (p.Arg247Ter)	Spermatogenic failure 66 [RCV005396331]	uncertain significance	7	50018284	50018284	Human	1	name
407487540	CV3420968	single nucleotide variant	NM_007009.3(ZPBP):c.1014A>T (p.Gln338His)	not specified [RCV004603789]	uncertain significance	7	49937570	49937570	Human		name
8632595	CV87810	single nucleotide variant	NM_001159878.1(ZPBP):c.524G>A (p.Arg175Gln)	Malignant melanoma [RCV000067902]	not provided	7	50031271	50031271	Human		name
401883713	CV2764501	single nucleotide variant	NM_199321.3(ZPBP2):c.80A>G (p.Asn27Ser)	not specified [RCV004339061]	uncertain significance	17	39868576	39868576	Human		name
15119147	CV715419	single nucleotide variant	NM_199321.3(ZPBP2):c.519T>C (p.Ser173=)	not provided [RCV000962499]	benign	17	39872382	39872382	Human		name
597748002	CV3646131	single nucleotide variant	NM_199321.3(ZPBP2):c.226A>G (p.Asn76Asp)	not specified [RCV004892051]	uncertain significance	17	39870801	39870801	Human		name
156313117	CV2256964	single nucleotide variant	NM_199321.3(ZPBP2):c.893T>C (p.Val298Ala)	not specified [RCV004121157]	uncertain significance	17	39876685	39876685	Human		name
155981548	CV2272866	single nucleotide variant	NM_199321.3(ZPBP2):c.733T>G (p.Phe245Val)	not specified [RCV004135769]	uncertain significance	17	39875278	39875278	Human		name
156285258	CV2291969	single nucleotide variant	NM_199321.3(ZPBP2):c.313G>A (p.Gly105Arg)	not specified [RCV004158478]	uncertain significance	17	39871532	39871532	Human		name
156279530	CV2297692	single nucleotide variant	NM_199321.3(ZPBP2):c.812A>G (p.Gln271Arg)	not specified [RCV004155374]	uncertain significance	17	39875357	39875357	Human		name
156303312	CV2331825	single nucleotide variant	NM_199321.3(ZPBP2):c.615A>G (p.Ile205Met)	not specified [RCV004184440]	uncertain significance	17	39872478	39872478	Human		name
155929031	CV2363415	single nucleotide variant	NM_199321.3(ZPBP2):c.342G>C (p.Lys114Asn)	not specified [RCV004215998]	uncertain significance	17	39871561	39871561	Human		name
401730124	CV2683961	single nucleotide variant	NM_199321.3(ZPBP2):c.821G>A (p.Arg274His)	not specified [RCV004286508]	uncertain significance	17	39875366	39875366	Human		name
401731446	CV2693810	single nucleotide variant	NM_199321.3(ZPBP2):c.497T>G (p.Val166Gly)	not specified [RCV004300124]	uncertain significance	17	39872360	39872360	Human		name
401742243	CV2718699	single nucleotide variant	NM_199321.3(ZPBP2):c.935G>T (p.Cys312Phe)	not specified [RCV004328457]	uncertain significance	17	39876727	39876727	Human		name
405675790	CV3354971	single nucleotide variant	NM_199321.3(ZPBP2):c.464G>A (p.Cys155Tyr)	not specified [RCV004487598]	uncertain significance	17	39872327	39872327	Human		name
405675795	CV3354972	single nucleotide variant	NM_199321.3(ZPBP2):c.553C>T (p.Pro185Ser)	not specified [RCV004487599]	uncertain significance	17	39872416	39872416	Human		name
405675800	CV3354973	single nucleotide variant	NM_199321.3(ZPBP2):c.665G>A (p.Gly222Glu)	not specified [RCV004487600]	uncertain significance	17	39873083	39873083	Human		name
407487557	CV3420971	single nucleotide variant	NM_199321.3(ZPBP2):c.413G>A (p.Arg138Gln)	not specified [RCV004603792]	uncertain significance	17	39872276	39872276	Human		name
407487565	CV3420972	single nucleotide variant	NM_199321.3(ZPBP2):c.761A>G (p.His254Arg)	not specified [RCV004603793]	uncertain significance	17	39875306	39875306	Human		name
407487571	CV3420973	single nucleotide variant	NM_199321.3(ZPBP2):c.399G>C (p.Met133Ile)	not specified [RCV004603794]	uncertain significance	17	39871618	39871618	Human		name
15119141	CV715418	single nucleotide variant	NM_199321.3(ZPBP2):c.352G>A (p.Ala118Thr)	not provided [RCV000962498]	benign	17	39871571	39871571	Human		name
15102682	CV727141	single nucleotide variant	NM_199321.3(ZPBP2):c.850A>G (p.Lys284Glu)	not provided [RCV000892528]	likely benign	17	39875395	39875395	Human		name
156271911	CV2315845	single nucleotide variant	NM_199321.3(ZPBP2):c.1011A>C (p.Glu337Asp)	not specified [RCV004171623]	uncertain significance	17	39876803	39876803	Human		name
156230279	CV2348667	single nucleotide variant	NM_199321.3(ZPBP2):c.1012G>A (p.Asp338Asn)	not specified [RCV004201086]	uncertain significance	17	39876804	39876804	Human		name

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