Spock3 Variant Search Result - Rat Genome Database

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42 records found for search term Spock3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8631080	CV86236	single nucleotide variant	NM_016950.2(SPOCK3):c.1142-2A>T	Malignant melanoma [RCV000066327]	not provided	4	166735092	166735092	Human		name
8579372	CV113772	single nucleotide variant	NM_016950.2(SPOCK3):c.718+3060T>C	Lung cancer [RCV000094295]	uncertain significance	4	166789110	166789110	Human		name
8579373	CV113773	single nucleotide variant	NM_016950.2(SPOCK3):c.199-4656G>T	Lung cancer [RCV000094296]	uncertain significance	4	167067193	167067193	Human		name
8579374	CV113774	single nucleotide variant	NM_016950.2(SPOCK3):c.190-75302G>T	Lung cancer [RCV000094297]	uncertain significance	4	167158548	167158548	Human		name
405737554	CV3333782	single nucleotide variant	NM_001040159.2(SPOCK3):c.7A>G (p.Lys3Glu)	not specified [RCV004465182]	uncertain significance	4	167234167	167234167	Human		name
405737566	CV3333784	single nucleotide variant	NM_001040159.2(SPOCK3):c.9G>T (p.Lys3Asn)	not specified [RCV004465184]	uncertain significance	4	167234165	167234165	Human		name
155971398	CV2262333	single nucleotide variant	NM_001040159.2(SPOCK3):c.26G>A (p.Cys9Tyr)	not specified [RCV004128526]	uncertain significance	4	167234148	167234148	Human		name
15099455	CV698429	single nucleotide variant	NM_001040159.2(SPOCK3):c.291A>G (p.Val97=)	not provided [RCV000958764]	benign	4	167000408	167000408	Human		name
8631081	CV86237	single nucleotide variant	NM_016950.2(SPOCK3):c.805G>A (p.Asp269Asn)	Malignant melanoma [RCV000066328]	not provided	4	166754643	166754643	Human		name
405737560	CV3333783	single nucleotide variant	NM_001040159.2(SPOCK3):c.88G>A (p.Gly30Arg)	not specified [RCV004465183]	uncertain significance	4	167234086	167234086	Human		name
407511587	CV3477971	single nucleotide variant	NM_001040159.2(SPOCK3):c.62C>T (p.Ala21Val)	not specified [RCV004673152]	uncertain significance	4	167234112	167234112	Human		name
156262441	CV2390870	single nucleotide variant	NM_001040159.2(SPOCK3):c.209G>T (p.Trp70Leu)	not specified [RCV004234891]	uncertain significance	4	167062518	167062518	Human		name
405737524	CV3333777	single nucleotide variant	NM_001040159.2(SPOCK3):c.160G>A (p.Glu54Lys)	not specified [RCV004465177]	uncertain significance	4	167234014	167234014	Human		name
405737530	CV3333778	single nucleotide variant	NM_001040159.2(SPOCK3):c.203G>A (p.Arg68His)	not specified [RCV004465178]	uncertain significance	4	167062524	167062524	Human		name
407511584	CV3477970	single nucleotide variant	NM_001040159.2(SPOCK3):c.281G>A (p.Arg94His)	not specified [RCV004673151]	uncertain significance	4	167000418	167000418	Human		name
598272228	CV3915501	single nucleotide variant	NM_001040159.2(SPOCK3):c.181T>C (p.Phe61Leu)	not specified [RCV005282553]	uncertain significance	4	167233993	167233993	Human		name
15202139	CV764378	single nucleotide variant	NM_001040159.2(SPOCK3):c.1152C>T (p.Ser384=)	not provided [RCV000935860]	likely benign	4	166735071	166735071	Human		name
156171155	CV2247428	single nucleotide variant	NM_001040159.2(SPOCK3):c.299C>T (p.Ala100Val)	not specified [RCV004108759]	uncertain significance	4	167000400	167000400	Human		name
156342053	CV2268353	single nucleotide variant	NM_001040159.2(SPOCK3):c.334C>T (p.Arg112Trp)	not specified [RCV004599525]	uncertain significance	4	167000365	167000365	Human		name
156272073	CV2297105	single nucleotide variant	NM_001040159.2(SPOCK3):c.394A>G (p.Ile132Val)	not specified [RCV004151014]	uncertain significance	4	166912700	166912700	Human		name
156061185	CV2380210	single nucleotide variant	NM_001040159.2(SPOCK3):c.638G>C (p.Trp213Ser)	not specified [RCV004224576]	uncertain significance	4	166792241	166792241	Human		name
401722568	CV2677035	single nucleotide variant	NM_001040159.2(SPOCK3):c.933C>A (p.Asp311Glu)	not specified [RCV004293634]	uncertain significance	4	166742058	166742058	Human		name
401889539	CV2758177	single nucleotide variant	NM_001040159.2(SPOCK3):c.971G>A (p.Arg324Gln)	not specified [RCV004341547]	uncertain significance	4	166742020	166742020	Human		name
405737535	CV3333779	single nucleotide variant	NM_001040159.2(SPOCK3):c.632G>A (p.Arg211Gln)	not specified [RCV004465179]	uncertain significance	4	166792247	166792247	Human		name
405737542	CV3333780	single nucleotide variant	NM_001040159.2(SPOCK3):c.647C>A (p.Ala216Asp)	not specified [RCV004465180]	uncertain significance	4	166792232	166792232	Human		name
405737547	CV3333781	single nucleotide variant	NM_001040159.2(SPOCK3):c.782A>G (p.Tyr261Cys)	not specified [RCV004465181]	uncertain significance	4	166754657	166754657	Human		name
407516492	CV3477973	single nucleotide variant	NM_001040159.2(SPOCK3):c.845C>A (p.Thr282Asn)	not specified [RCV004675128]	uncertain significance	4	166754594	166754594	Human		name
597769037	CV3607740	single nucleotide variant	NM_001040159.2(SPOCK3):c.619G>A (p.Ala207Thr)	not specified [RCV004871161]	uncertain significance	4	166792260	166792260	Human		name
597679132	CV3607743	single nucleotide variant	NM_001040159.2(SPOCK3):c.461C>G (p.Thr154Ser)	not specified [RCV004857271]	uncertain significance	4	166912633	166912633	Human		name
15165835	CV698428	single nucleotide variant	NM_001040159.2(SPOCK3):c.325A>G (p.Ile109Val)	not provided [RCV000948688]	benign	4	167000374	167000374	Human		name
156322479	CV2205073	single nucleotide variant	NM_001040159.2(SPOCK3):c.1214T>C (p.Ile405Thr)	not specified [RCV004077680]	uncertain significance	4	166735009	166735009	Human		name
156209597	CV2304528	single nucleotide variant	NM_001040159.2(SPOCK3):c.1280A>G (p.Asp427Gly)	not specified [RCV004164608]	uncertain significance	4	166734943	166734943	Human		name
401726870	CV2691877	single nucleotide variant	NM_001040159.2(SPOCK3):c.1124C>T (p.Ala375Val)	not specified [RCV004299617]	uncertain significance	4	166737475	166737475	Human		name
401746425	CV2694853	single nucleotide variant	NM_001040159.2(SPOCK3):c.1257A>C (p.Glu419Asp)	not specified [RCV004300928]	uncertain significance	4	166734966	166734966	Human		name
401880985	CV2789453	single nucleotide variant	NM_001040159.2(SPOCK3):c.1148T>A (p.Ile383Asn)	not specified [RCV004360085]	uncertain significance	4	166735075	166735075	Human		name
405737498	CV3323401	single nucleotide variant	NM_001040159.2(SPOCK3):c.1049A>G (p.His350Arg)	not specified [RCV004465173]	uncertain significance	4	166737550	166737550	Human		name
405737507	CV3333774	single nucleotide variant	NM_001040159.2(SPOCK3):c.1096G>A (p.Val366Ile)	not specified [RCV004465174]	uncertain significance	4	166737503	166737503	Human		name
405737515	CV3333775	single nucleotide variant	NM_001040159.2(SPOCK3):c.1209C>A (p.Asp403Glu)	not specified [RCV004465175]	uncertain significance	4	166735014	166735014	Human		name
405737521	CV3333776	single nucleotide variant	NM_001040159.2(SPOCK3):c.1286A>G (p.His429Arg)	not specified [RCV004465176]	uncertain significance	4	166734937	166734937	Human		name
407511590	CV3477972	single nucleotide variant	NM_001040159.2(SPOCK3):c.1198G>A (p.Asp400Asn)	not specified [RCV004673153]	uncertain significance	4	166735025	166735025	Human		name
597679123	CV3607742	single nucleotide variant	NM_001040159.2(SPOCK3):c.1297A>G (p.Ile433Val)	not specified [RCV004857270]	uncertain significance	4	166734926	166734926	Human		name
15165832	CV698427	single nucleotide variant	NM_001040159.2(SPOCK3):c.1298T>A (p.Ile433Asn)	not provided [RCV000948687]	benign	4	166734925	166734925	Human		name

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