Crh Variant Search Result - Rat Genome Database

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158 records found for search term Crh

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8654872	CV49459	single nucleotide variant	NM_000756.3(CRH):c.-365G>C	Autosomal dominant nocturnal frontal lobe epilepsy [RCV000033934]	pathogenic\|likely pathogenic\|not provided	8	66178643	66178643	Human	1	name
13809162	CV577070	single nucleotide variant	NM_000756.4(CRH):c.51G>C (p.Leu17=)	not provided [RCV000711325]\|not specified [RCV004026803]	benign	8	66177427	66177427	Human		name
13828452	CV579692	single nucleotide variant	NM_000756.4(CRH):c.72G>A (p.Ala24=)	not provided [RCV004707405]\|not specified [RCV004026852]	likely benign	8	66177406	66177406	Human		name
150435833	CV1246516	single nucleotide variant	NM_000756.4(CRH):c.123T>G (p.Pro41=)	not specified [RCV001665515]	likely benign	8	66177355	66177355	Human		name
13809158	CV577069	single nucleotide variant	NM_000756.4(CRH):c.288A>C (p.Gly96=)	not provided [RCV000711323]\|not specified [RCV004026801]	benign	8	66177190	66177190	Human		name
155736296	CV1798665	single nucleotide variant	NM_000756.4(CRH):c.468G>A (p.Glu156=)	not specified [RCV004051986]	likely benign	8	66177010	66177010	Human		name
10049291	CV181175	single nucleotide variant	NM_000756.4(CRH):c.89C>G (p.Pro30Arg)	Autosomal dominant nocturnal frontal lobe epilepsy [RCV000192059]\|not provided [RCV000172993]\|not specified [RCV004019949]	pathogenic\|likely benign\|uncertain significance\|not provided	8	66177389	66177389	Human	1	name
155670419	CV1819175	single nucleotide variant	NM_000756.4(CRH):c.70G>A (p.Ala24Thr)	not specified [RCV004055257]	uncertain significance	8	66177408	66177408	Human		name
155714785	CV1820867	single nucleotide variant	NM_000756.4(CRH):c.85G>A (p.Gly29Arg)	not specified [RCV004056546]	uncertain significance	8	66177393	66177393	Human		name
156280076	CV2315948	single nucleotide variant	NM_000756.4(CRH):c.52C>T (p.Pro18Ser)	not specified [RCV004172019]	uncertain significance	8	66177426	66177426	Human		name
13809159	CV577068	single nucleotide variant	NM_000756.4(CRH):c.456G>A (p.Arg152=)	CRH-related disorder [RCV003907967]\|not provided [RCV000711324]\|not specified [RCV004026802]	benign\|likely benign	8	66177022	66177022	Human		name , trait , alternate_id
13830785	CV579481	single nucleotide variant	NM_000756.4(CRH):c.579T>C (p.Ile193=)	not specified [RCV004026916]	likely benign	8	66176899	66176899	Human		name
13828488	CV579485	single nucleotide variant	NM_000756.4(CRH):c.438G>A (p.Glu146=)	not specified [RCV004026855]	likely benign	8	66177040	66177040	Human		name
15112656	CV723168	single nucleotide variant	NM_000756.4(CRH):c.378C>G (p.Leu126=)	not provided [RCV000894512]	likely benign	8	66177100	66177100	Human		name
155669679	CV1846786	single nucleotide variant	NM_000756.4(CRH):c.202A>T (p.Met68Leu)	not specified [RCV004059562]	uncertain significance	8	66177276	66177276	Human		name
597773934	CV3661293	single nucleotide variant	NM_000756.4(CRH):c.107A>G (p.Gln36Arg)	not specified [RCV004897641]	uncertain significance	8	66177371	66177371	Human		name
597670429	CV3661294	single nucleotide variant	NM_000756.4(CRH):c.290G>T (p.Gly97Val)	not specified [RCV004913084]	uncertain significance	8	66177188	66177188	Human		name
597670437	CV3661295	single nucleotide variant	NM_000756.4(CRH):c.266C>A (p.Pro89His)	not specified [RCV004913085]	uncertain significance	8	66177212	66177212	Human		name
597773929	CV3661296	single nucleotide variant	NM_000756.4(CRH):c.161A>C (p.Glu54Ala)	not specified [RCV004897642]	uncertain significance	8	66177317	66177317	Human		name
597670444	CV3661297	single nucleotide variant	NM_000756.4(CRH):c.200G>A (p.Arg67His)	not specified [RCV004913086]	uncertain significance	8	66177278	66177278	Human		name
597670462	CV3661299	single nucleotide variant	NM_000756.4(CRH):c.295G>A (p.Gly99Ser)	not specified [RCV004913088]	uncertain significance	8	66177183	66177183	Human		name
598249281	CV3941743	single nucleotide variant	NM_000756.4(CRH):c.197T>A (p.Leu66His)	not specified [RCV005322722]	uncertain significance	8	66177281	66177281	Human		name
13828337	CV579466	single nucleotide variant	NM_000756.4(CRH):c.239A>G (p.Asn80Ser)	not specified [RCV004026844]	uncertain significance	8	66177239	66177239	Human		name
13828267	CV579493	single nucleotide variant	NM_000756.4(CRH):c.110C>T (p.Ala37Val)	not specified [RCV004026839]	uncertain significance	8	66177368	66177368	Human		name
155717065	CV1792124	single nucleotide variant	NM_000756.4(CRH):c.329A>G (p.Asn110Ser)	not specified [RCV004049488]	likely benign\|uncertain significance	8	66177149	66177149	Human		name
156078741	CV2230379	single nucleotide variant	NM_000756.4(CRH):c.394C>G (p.Leu132Val)	not specified [RCV004099973]	uncertain significance	8	66177084	66177084	Human		name
155932264	CV2232041	single nucleotide variant	NM_000756.4(CRH):c.529G>A (p.Ala177Thr)	not specified [RCV004093090]	uncertain significance	8	66176949	66176949	Human		name
155901748	CV2274569	single nucleotide variant	NM_000756.4(CRH):c.367C>G (p.Arg123Gly)	not specified [RCV004138967]	uncertain significance	8	66177111	66177111	Human		name
155903306	CV2301617	single nucleotide variant	NM_000756.4(CRH):c.421C>G (p.Leu141Val)	not specified [RCV004162523]	uncertain significance	8	66177057	66177057	Human		name
329377259	CV2442697	single nucleotide variant	NM_000756.4(CRH):c.340G>C (p.Val114Leu)	not specified [RCV004265042]	uncertain significance	8	66177138	66177138	Human		name
401761438	CV2702336	single nucleotide variant	NM_000756.4(CRH):c.424G>A (p.Gly142Ser)	not specified [RCV004316866]	uncertain significance	8	66177054	66177054	Human		name
405664190	CV3242745	single nucleotide variant	NM_000756.4(CRH):c.522G>C (p.Met174Ile)	not specified [RCV004367286]	uncertain significance	8	66176956	66176956	Human		name
407463849	CV3419929	single nucleotide variant	NM_000756.4(CRH):c.419C>G (p.Ala140Gly)	not specified [RCV004613298]	uncertain significance	8	66177059	66177059	Human		name
597670453	CV3661298	single nucleotide variant	NM_000756.4(CRH):c.437A>C (p.Glu146Ala)	not specified [RCV004913087]	uncertain significance	8	66177041	66177041	Human		name
13828298	CV579503	microsatellite	NM_000756.4(CRH):c.146CGC[4] (p.Pro51dup)	not provided [RCV000953582]\|not specified [RCV004026842]	benign	8	66177323	66177324	Human		name
155720172	CV1830691	duplication	NM_000756.4(CRH):c.157_180dup (p.Gln60_Ala61insSerGluGlnProGlnGlnProGln)	not specified [RCV004059191]	uncertain significance	8	66177297	66177298	Human		name
8604580	CV47403	single nucleotide variant	NC_000008.11:g.66178947G>T	Autosomal dominant nocturnal frontal lobe epilepsy [RCV000033935]\|CRH-related disorder [RCV003894839]	pathogenic\|likely benign\|not provided	8	66178947	66178947	Human	1	trait , alternate_id
150502483	CV1212244	single nucleotide variant	NM_004382.5(CRHR1):c.*212G>A	not provided [RCV001595117]	benign	17	45834976	45834976	Human		name
15199468	CV759678	single nucleotide variant	NM_001883.5(CRHR2):c.832-5T>A	not provided [RCV000912555]	likely benign	7	30656017	30656017	Human		name
15113447	CV780110	single nucleotide variant	NM_004382.5(CRHR1):c.435-10G>A	not provided [RCV000961493]	benign	17	45830084	45830084	Human		name
405280769	CV3195738	single nucleotide variant	NM_004382.5(CRHR1):c.434+293C>A	CRHR1-related disorder [RCV003906970]	likely benign	17	45829614	45829614	Human		name , trait , alternate_id
405267497	CV3219362	single nucleotide variant	NM_004382.5(CRHR1):c.434+292G>T	CRHR1-related disorder [RCV003969612]	likely benign	17	45829613	45829613	Human		name , trait , alternate_id
11087696	CV227791	single nucleotide variant	NM_004382.5(CRHR1):c.1107+111C>T	budesonide response - Efficacy [RCV000211373]\|corticosteroids response - Efficacy [RCV000211194]\|fluticasone propionate response - Efficacy [RCV000211279]\|fluticasone/salmeterol response - Efficacy [RCV000211365]\|triamcinolone response - Efficacy [RCV000211182]	drug response	17	45834159	45834159	Human		name
11087744	CV227761	single nucleotide variant	NM_001202481.1(CRHR2):c.-166-546T>A	salbutamol response - Efficacy [RCV000211260]\|selective beta-2-adrenoreceptor agonists response - Efficacy [RCV000211347]	drug response	7	30687161	30687161	Human		name
8632542	CV87750	single nucleotide variant	NM_001202481.1(CRHR2):c.-167+225C>T	Malignant melanoma [RCV000067842]	not provided	7	30688966	30688966	Human		name
8585373	CV119959	single nucleotide variant	NM_001256299.2(MGC57346-CRHR1):c.-493+20112C>A	Lung cancer [RCV000100479]	uncertain significance	17	45650270	45650270	Human		name
8585374	CV119960	single nucleotide variant	NM_001256299.2(MGC57346-CRHR1):c.-493+20378G>T	Lung cancer [RCV000100480]	uncertain significance	17	45650536	45650536	Human		name
8585375	CV119961	single nucleotide variant	NM_001256299.2(MGC57346-CRHR1):c.-492-27302A>G	Lung cancer [RCV000100481]	uncertain significance	17	45779708	45779708	Human		name
407478162	CV3419939	single nucleotide variant	NM_004382.5(CRHR1):c.23G>A (p.Arg8His)	not specified [RCV004613308]	uncertain significance	17	45784567	45784567	Human		name
15188116	CV699169	single nucleotide variant	NM_001882.4(CRHBP):c.267C>G (p.Pro89=)	not provided [RCV000953786]	benign	5	76954120	76954120	Human		name
15162315	CV704182	single nucleotide variant	NM_004382.5(CRHR1):c.177T>C (p.Pro59=)	not provided [RCV000947832]	benign	17	45816518	45816518	Human		name
15168824	CV721535	single nucleotide variant	NM_001882.4(CRHBP):c.159G>A (p.Pro53=)	not provided [RCV000883145]	benign	5	76953678	76953678	Human		name
156117493	CV2278852	single nucleotide variant	NM_001882.4(CRHBP):c.40A>G (p.Ile14Val)	not specified [RCV004145560]	uncertain significance	5	76953174	76953174	Human		name
156149818	CV2394605	single nucleotide variant	NM_004382.5(CRHR1):c.61G>A (p.Val21Ile)	not specified [RCV004240952]	likely benign	17	45807037	45807037	Human		name
405664234	CV3242753	single nucleotide variant	NM_004382.5(CRHR1):c.34G>A (p.Ala12Thr)	not specified [RCV004367294]	uncertain significance	17	45807010	45807010	Human		name
405664254	CV3242757	single nucleotide variant	NM_004382.5(CRHR1):c.498C>T (p.Asn166=)	not specified [RCV004367298]	likely benign	17	45830157	45830157	Human		name
405664263	CV3242759	single nucleotide variant	NM_004382.5(CRHR1):c.96C>A (p.Ser32Arg)	not specified [RCV004367300]	uncertain significance	17	45807072	45807072	Human		name
15150761	CV727236	single nucleotide variant	NM_004382.5(CRHR1):c.579C>T (p.Ala193=)	not provided [RCV000879450]	benign	17	45830440	45830440	Human		name
15162987	CV755907	single nucleotide variant	NM_004382.5(CRHR1):c.312G>A (p.Glu104=)	not provided [RCV000926017]	likely benign	17	45821425	45821425	Human		name
8689328	CV97415	single nucleotide variant	NM_001883.5(CRHR2):c.915C>T (p.Tyr305=)	not provided [RCV000122495]	uncertain significance	7	30655929	30655929	Human		name
155962847	CV2285701	single nucleotide variant	NM_001882.4(CRHBP):c.149G>C (p.Gly50Ala)	not specified [RCV004141549]	uncertain significance	5	76953668	76953668	Human		name
156301896	CV2307116	single nucleotide variant	NM_001882.4(CRHBP):c.292G>C (p.Asp98His)	not specified [RCV004159597]	uncertain significance	5	76954145	76954145	Human		name
156127850	CV2351279	single nucleotide variant	NM_001883.5(CRHR2):c.197A>C (p.Glu66Ala)	not specified [RCV004214125]	uncertain significance	7	30681947	30681947	Human		name
156092882	CV2381977	single nucleotide variant	NM_004382.5(CRHR1):c.184C>A (p.Gln62Lys)	not specified [RCV004225908]	uncertain significance	17	45816525	45816525	Human		name
156159002	CV2398079	single nucleotide variant	NM_004382.5(CRHR1):c.283G>A (p.Ala95Thr)	not specified [RCV004241666]	uncertain significance	17	45821396	45821396	Human		name
401723866	CV2725065	single nucleotide variant	NM_001883.5(CRHR2):c.196G>A (p.Glu66Lys)	not specified [RCV004319818]	uncertain significance	7	30681948	30681948	Human		name
405664196	CV3242746	single nucleotide variant	NM_001882.4(CRHBP):c.176G>A (p.Arg59Gln)	not specified [RCV004367287]	uncertain significance	5	76954029	76954029	Human		name
405664201	CV3242747	single nucleotide variant	NM_001882.4(CRHBP):c.223G>A (p.Asp75Asn)	not specified [RCV004367288]	uncertain significance	5	76954076	76954076	Human		name
405664206	CV3242748	single nucleotide variant	NM_001882.4(CRHBP):c.227G>T (p.Arg76Leu)	not specified [RCV004367289]	uncertain significance	5	76954080	76954080	Human		name
405664227	CV3242752	single nucleotide variant	NM_004382.5(CRHR1):c.142G>A (p.Val48Met)	not specified [RCV004367293]	uncertain significance	17	45816483	45816483	Human		name
407463858	CV3419931	single nucleotide variant	NM_001882.4(CRHBP):c.240C>G (p.His80Gln)	not specified [RCV004613300]	uncertain significance	5	76954093	76954093	Human		name
597670510	CV3661305	single nucleotide variant	NM_004382.5(CRHR1):c.169C>T (p.Arg57Cys)	not specified [RCV004913094]	uncertain significance	17	45816510	45816510	Human		name
597670600	CV3661316	single nucleotide variant	NM_001883.5(CRHR2):c.143G>C (p.Gly48Ala)	not specified [RCV004913105]	uncertain significance	7	30682001	30682001	Human		name
597670617	CV3661318	single nucleotide variant	NM_001883.5(CRHR2):c.191G>T (p.Cys64Phe)	not specified [RCV004913107]	uncertain significance	7	30681953	30681953	Human		name
597671580	CV3661322	single nucleotide variant	NM_001883.5(CRHR2):c.150C>G (p.Cys50Trp)	not specified [RCV004913111]	uncertain significance	7	30681994	30681994	Human		name
598249325	CV3941749	single nucleotide variant	NM_004382.5(CRHR1):c.194T>C (p.Val65Ala)	not specified [RCV005322728]	uncertain significance	17	45816535	45816535	Human		name
15100469	CV700033	single nucleotide variant	NM_001202475.1(CRHR2):c.96C>T (p.Ala32=)	not provided [RCV000958919]	benign	7	30689279	30689279	Human		name
15177878	CV704183	single nucleotide variant	NM_004382.5(CRHR1):c.179C>T (p.Ala60Val)	not provided [RCV000951143]	benign	17	45816520	45816520	Human	1	name
15177878	CV704183	single nucleotide variant	NM_004382.5(CRHR1):c.179C>T (p.Ala60Val)	not provided [RCV000951143]	benign	17	45816520	45816521	Human	1	name
156329351	CV2213821	single nucleotide variant	NM_001883.5(CRHR2):c.904A>G (p.Thr302Ala)	not specified [RCV004089878]	uncertain significance	7	30655940	30655940	Human		name
156385622	CV2227983	single nucleotide variant	NM_001883.5(CRHR2):c.577T>A (p.Tyr193Asn)	not specified [RCV004096231]	uncertain significance	7	30662814	30662814	Human		name
156236010	CV2245479	single nucleotide variant	NM_001883.5(CRHR2):c.580T>A (p.Phe194Ile)	not specified [RCV004109257]	uncertain significance	7	30662811	30662811	Human		name
156079795	CV2259249	single nucleotide variant	NM_001883.5(CRHR2):c.662G>A (p.Arg221His)	not specified [RCV004122271]	uncertain significance	7	30662729	30662729	Human		name
155987837	CV2259509	single nucleotide variant	NM_001882.4(CRHBP):c.706G>A (p.Gly236Ser)	not specified [RCV004122704]	uncertain significance	5	76963355	76963355	Human		name
155905110	CV2285846	single nucleotide variant	NM_001883.5(CRHR2):c.661C>T (p.Arg221Cys)	not specified [RCV004143789]	uncertain significance	7	30662730	30662730	Human		name
156085091	CV2295236	single nucleotide variant	NM_001883.5(CRHR2):c.337T>C (p.Tyr113His)	not specified [RCV004158619]	uncertain significance	7	30665618	30665618	Human		name
156242248	CV2306495	single nucleotide variant	NM_001883.5(CRHR2):c.709C>T (p.Pro237Ser)	not specified [RCV004157112]	uncertain significance	7	30662205	30662205	Human		name
155981785	CV2351427	single nucleotide variant	NM_001883.5(CRHR2):c.890C>T (p.Ser297Phe)	not specified [RCV004193115]	uncertain significance	7	30655954	30655954	Human		name
156269501	CV2379304	single nucleotide variant	NM_001883.5(CRHR2):c.971T>C (p.Met324Thr)	not specified [RCV004223771]	uncertain significance	7	30655662	30655662	Human		name
156205938	CV2385265	single nucleotide variant	NM_001882.4(CRHBP):c.913G>A (p.Glu305Lys)	not specified [RCV004228506]	uncertain significance	5	76968829	76968829	Human		name
401730844	CV2677363	single nucleotide variant	NM_001882.4(CRHBP):c.720A>G (p.Ile240Met)	not specified [RCV004289070]	uncertain significance	5	76963369	76963369	Human		name
401730091	CV2683944	single nucleotide variant	NM_001883.5(CRHR2):c.784G>A (p.Asp262Asn)	not specified [RCV004284663]	uncertain significance	7	30660620	30660620	Human		name
401747365	CV2688895	single nucleotide variant	NM_004382.5(CRHR1):c.553G>A (p.Val185Met)	not specified [RCV004303903]	uncertain significance	17	45830212	45830212	Human		name
401728864	CV2693881	single nucleotide variant	NM_001883.5(CRHR2):c.698G>A (p.Cys233Tyr)	not specified [RCV004300181]	uncertain significance	7	30662216	30662216	Human		name
401744325	CV2696981	single nucleotide variant	NM_004382.5(CRHR1):c.871G>A (p.Val291Ile)	not specified [RCV004292973]	uncertain significance	17	45833479	45833479	Human		name
401752231	CV2710621	single nucleotide variant	NM_004382.5(CRHR1):c.526A>G (p.Met176Val)	not specified [RCV004319535]	uncertain significance	17	45830185	45830185	Human		name
401861710	CV2756438	single nucleotide variant	NM_001883.5(CRHR2):c.343A>G (p.Ile115Val)	not specified [RCV004342974]	likely benign	7	30665612	30665612	Human		name
401889425	CV2756510	single nucleotide variant	NM_001883.5(CRHR2):c.883C>T (p.Arg295Cys)	not specified [RCV004345042]	uncertain significance	7	30655961	30655961	Human		name
401879695	CV2769698	single nucleotide variant	NM_001882.4(CRHBP):c.880G>T (p.Val294Leu)	not specified [RCV004351619]	uncertain significance	5	76968796	76968796	Human		name
405664211	CV3242749	single nucleotide variant	NM_001882.4(CRHBP):c.368T>C (p.Phe123Ser)	not specified [RCV004367290]	uncertain significance	5	76955687	76955687	Human		name
405664218	CV3242750	single nucleotide variant	NM_001882.4(CRHBP):c.673G>A (p.Val225Ile)	not specified [RCV004367291]	uncertain significance	5	76958869	76958869	Human		name
405664244	CV3242755	single nucleotide variant	NM_004382.5(CRHR1):c.437G>A (p.Ser146Asn)	not specified [RCV004367296]	uncertain significance	17	45830096	45830096	Human		name
405664249	CV3242756	single nucleotide variant	NM_004382.5(CRHR1):c.442C>T (p.Arg148Trp)	not specified [RCV004367297]	uncertain significance	17	45830101	45830101	Human		name
405664257	CV3242758	single nucleotide variant	NM_004382.5(CRHR1):c.550A>G (p.Asn184Asp)	not specified [RCV004367299]	uncertain significance	17	45830209	45830209	Human		name
405664286	CV3242764	single nucleotide variant	NM_001883.5(CRHR2):c.414C>A (p.Phe138Leu)	not specified [RCV004367305]	uncertain significance	7	30665541	30665541	Human		name
405664291	CV3242765	single nucleotide variant	NM_001883.5(CRHR2):c.743A>G (p.Tyr248Cys)	not specified [RCV004367306]	uncertain significance	7	30662171	30662171	Human		name
405664295	CV3242766	single nucleotide variant	NM_001883.5(CRHR2):c.786C>G (p.Asp262Glu)	not specified [RCV004367307]	uncertain significance	7	30660618	30660618	Human		name
407463854	CV3419930	single nucleotide variant	NM_001882.4(CRHBP):c.712G>C (p.Glu238Gln)	not specified [RCV004613299]	uncertain significance	5	76963361	76963361	Human		name
407478129	CV3419933	single nucleotide variant	NM_004382.5(CRHR1):c.301G>A (p.Glu101Lys)	not specified [RCV004613302]	uncertain significance	17	45821414	45821414	Human		name
407478135	CV3419934	single nucleotide variant	NM_004382.5(CRHR1):c.543C>G (p.His181Gln)	not specified [RCV004613303]	likely benign	17	45830202	45830202	Human		name
407478147	CV3419936	single nucleotide variant	NM_004382.5(CRHR1):c.811A>G (p.Ile271Val)	not specified [RCV004613305]	uncertain significance	17	45833178	45833178	Human		name
407478151	CV3419937	single nucleotide variant	NM_004382.5(CRHR1):c.649A>G (p.Ile217Val)	not specified [RCV004613306]	likely benign	17	45830510	45830510	Human		name
407478158	CV3419938	single nucleotide variant	NM_004382.5(CRHR1):c.443G>A (p.Arg148Gln)	not specified [RCV004613307]	uncertain significance	17	45830102	45830102	Human		name
407463866	CV3419940	single nucleotide variant	NM_001883.5(CRHR2):c.583G>A (p.Val195Met)	not specified [RCV004613309]	uncertain significance	7	30662808	30662808	Human		name
407463874	CV3419942	single nucleotide variant	NM_001883.5(CRHR2):c.978C>A (p.Phe326Leu)	not specified [RCV004613311]	uncertain significance	7	30655655	30655655	Human		name
407463878	CV3419943	single nucleotide variant	NM_001883.5(CRHR2):c.753T>G (p.Asn251Lys)	not specified [RCV004613312]	uncertain significance	7	30662161	30662161	Human		name
597670477	CV3661301	single nucleotide variant	NM_001882.4(CRHBP):c.773C>T (p.Thr258Met)	not specified [RCV004913090]	likely benign	5	76963422	76963422	Human		name
597670486	CV3661302	single nucleotide variant	NM_001882.4(CRHBP):c.491A>G (p.His164Arg)	not specified [RCV004913091]	likely benign	5	76955810	76955810	Human		name
597670494	CV3661303	single nucleotide variant	NM_001882.4(CRHBP):c.536A>G (p.Asn179Ser)	not specified [RCV004913092]	uncertain significance	5	76955855	76955855	Human		name
597670501	CV3661304	single nucleotide variant	NM_004382.5(CRHR1):c.679C>T (p.Arg227Cys)	not specified [RCV004913093]	uncertain significance	17	45830540	45830540	Human		name
597670519	CV3661306	single nucleotide variant	NM_004382.5(CRHR1):c.982A>G (p.Met328Val)	not specified [RCV004913095]	uncertain significance	17	45833766	45833766	Human		name
597670528	CV3661307	single nucleotide variant	NM_004382.5(CRHR1):c.778T>C (p.Phe260Leu)	not specified [RCV004913096]	uncertain significance	17	45833145	45833145	Human		name
597670536	CV3661308	single nucleotide variant	NM_004382.5(CRHR1):c.875G>T (p.Arg292Leu)	not specified [RCV004913097]	uncertain significance	17	45833483	45833483	Human		name
597670545	CV3661309	single nucleotide variant	NM_004382.5(CRHR1):c.806A>G (p.Asp269Gly)	not specified [RCV004913098]	uncertain significance	17	45833173	45833173	Human		name
597670564	CV3661311	single nucleotide variant	NM_004382.5(CRHR1):c.331A>G (p.Lys111Glu)	not specified [RCV004913100]	uncertain significance	17	45829218	45829218	Human		name
597670570	CV3661312	single nucleotide variant	NM_004382.5(CRHR1):c.515T>C (p.Val172Ala)	not specified [RCV004913101]	uncertain significance	17	45830174	45830174	Human		name
597670577	CV3661313	single nucleotide variant	NM_004382.5(CRHR1):c.691T>C (p.Phe231Leu)	not specified [RCV004913102]	uncertain significance	17	45830552	45830552	Human		name
597670584	CV3661314	single nucleotide variant	NM_001883.5(CRHR2):c.442C>T (p.Arg148Trp)	not specified [RCV004913103]	uncertain significance	7	30665171	30665171	Human		name
597670609	CV3661317	single nucleotide variant	NM_001883.5(CRHR2):c.632C>T (p.Thr211Met)	not specified [RCV004913106]	uncertain significance	7	30662759	30662759	Human		name
597671605	CV3661319	single nucleotide variant	NM_001883.5(CRHR2):c.781G>A (p.Gly261Ser)	not specified [RCV004913108]	uncertain significance	7	30660623	30660623	Human		name
597671588	CV3661321	single nucleotide variant	NM_001883.5(CRHR2):c.424C>T (p.Arg142Trp)	not specified [RCV004913110]	uncertain significance	7	30665531	30665531	Human		name
598249288	CV3941744	single nucleotide variant	NM_001882.4(CRHBP):c.478T>A (p.Phe160Ile)	not specified [RCV005322723]	uncertain significance	5	76955797	76955797	Human		name
598249294	CV3941745	single nucleotide variant	NM_001882.4(CRHBP):c.655G>C (p.Asp219His)	not specified [RCV005322724]	uncertain significance	5	76958851	76958851	Human		name
598249301	CV3941746	single nucleotide variant	NM_004382.5(CRHR1):c.580G>A (p.Ala194Thr)	not specified [RCV005322725]	uncertain significance	17	45830441	45830441	Human		name
598249318	CV3941748	single nucleotide variant	NM_004382.5(CRHR1):c.646G>A (p.Ala216Thr)	not specified [RCV005322727]	uncertain significance	17	45830507	45830507	Human		name
598249348	CV3941752	single nucleotide variant	NM_001883.5(CRHR2):c.653C>T (p.Ser218Phe)	not specified [RCV005322731]	uncertain significance	7	30662738	30662738	Human		name
598160155	CV3941754	single nucleotide variant	NM_001883.5(CRHR2):c.448G>A (p.Val150Met)	not specified [RCV005328711]	uncertain significance	7	30665165	30665165	Human		name
598249361	CV3941755	single nucleotide variant	NM_001883.5(CRHR2):c.517G>A (p.Asp173Asn)	not specified [RCV005322733]	uncertain significance	7	30665096	30665096	Human		name
15145825	CV736110	single nucleotide variant	NM_001883.5(CRHR2):c.920A>G (p.Lys307Arg)	not provided [RCV000900222]	likely benign	7	30655713	30655713	Human		name
155950988	CV2238693	single nucleotide variant	NM_001883.5(CRHR2):c.1011G>C (p.Gln337His)	not specified [RCV004107587]	uncertain significance	7	30655622	30655622	Human		name
156147209	CV2289348	single nucleotide variant	NM_001883.5(CRHR2):c.1180C>T (p.Pro394Ser)	not specified [RCV004152317]	uncertain significance	7	30653516	30653516	Human		name
155927912	CV2349848	single nucleotide variant	NM_004382.5(CRHR1):c.1027G>A (p.Val343Ile)	not specified [RCV004206272]	uncertain significance	17	45833811	45833811	Human		name
156344319	CV2364262	single nucleotide variant	NM_004382.5(CRHR1):c.1138C>T (p.Arg380Trp)	not specified [RCV004223492]	uncertain significance	17	45834654	45834654	Human		name
156149151	CV2394553	single nucleotide variant	NM_004382.5(CRHR1):c.1021C>T (p.Arg341Trp)	not specified [RCV004240906]	uncertain significance	17	45833805	45833805	Human		name
401880725	CV2780063	single nucleotide variant	NM_001883.5(CRHR2):c.1030A>G (p.Asn344Asp)	not specified [RCV004355727]	uncertain significance	7	30655603	30655603	Human		name
401935792	CV2811426	single nucleotide variant	NM_004382.5(CRHR1):c.1171G>A (p.Val391Met)	not provided [RCV003413254]	benign	17	45834687	45834687	Human		name
405664222	CV3242751	single nucleotide variant	NM_004382.5(CRHR1):c.1147G>A (p.Asp383Asn)	not specified [RCV004367292]	uncertain significance	17	45834663	45834663	Human		name
405664271	CV3242761	single nucleotide variant	NM_001883.5(CRHR2):c.1099C>T (p.Arg367Cys)	not specified [RCV004367302]	uncertain significance	7	30653597	30653597	Human		name
405664277	CV3242762	single nucleotide variant	NM_001883.5(CRHR2):c.1223C>T (p.Thr408Met)	not specified [RCV004367303]	uncertain significance	7	30653473	30653473	Human		name
407478140	CV3419935	single nucleotide variant	NM_004382.5(CRHR1):c.1111C>T (p.Arg371Cys)	not specified [RCV004613304]	uncertain significance	17	45834627	45834627	Human		name
407463870	CV3419941	single nucleotide variant	NM_001883.5(CRHR2):c.1134G>T (p.Gln378His)	not specified [RCV004613310]	uncertain significance	7	30653562	30653562	Human		name
597670591	CV3661315	single nucleotide variant	NM_001883.5(CRHR2):c.1195C>T (p.Arg399Trp)	not specified [RCV004913104]	uncertain significance	7	30653501	30653501	Human		name
598249309	CV3941747	single nucleotide variant	NM_004382.5(CRHR1):c.1036T>C (p.Tyr346His)	not specified [RCV005322726]	uncertain significance	17	45833820	45833820	Human		name
598249333	CV3941750	single nucleotide variant	NM_001883.5(CRHR2):c.1228G>A (p.Ala410Thr)	not specified [RCV005322729]	likely benign	7	30653468	30653468	Human		name
598249340	CV3941751	single nucleotide variant	NM_001883.5(CRHR2):c.1126C>T (p.Arg376Cys)	not specified [RCV005322730]	uncertain significance	7	30653570	30653570	Human		name
15115020	CV710972	single nucleotide variant	NM_001883.5(CRHR2):c.1231G>A (p.Val411Met)	not provided [RCV000961778]	benign	7	30653465	30653465	Human		name
156224203	CV2229736	single nucleotide variant	NM_001202475.1(CRHR2):c.108G>C (p.Gln36His)	not specified [RCV004103536]	uncertain significance	7	30689267	30689267	Human		name
8626408	CV81552	single nucleotide variant	NM_001202481.1(CRHR2):c.1154G>A (p.Arg385Gln)	Malignant melanoma [RCV000061630]	not provided	7	30653500	30653500	Human		name

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