Prc1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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78 records found for search term Prc1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
9850460	CV167494	single nucleotide variant	NM_003981.4(PRC1):c.*627T>C	Familial cancer of breast [RCV000162270]	uncertain significance	15	90966504	90966504	Human	1	name
9850461	CV167495	single nucleotide variant	NM_003981.4(PRC1):c.*769A>G	Familial cancer of breast [RCV000162271]	uncertain significance	15	90966362	90966362	Human	1	name
9850463	CV167497	single nucleotide variant	NM_003981.4(PRC1):c.*342A>G	Familial cancer of breast [RCV000162273]	uncertain significance	15	90966789	90966789	Human	1	name
9850464	CV167498	single nucleotide variant	NM_003981.4(PRC1):c.*441C>A	Familial cancer of breast [RCV000162274]	uncertain significance	15	90966690	90966690	Human	1	name
9850465	CV167499	single nucleotide variant	NM_003981.4(PRC1):c.*733G>A	Familial cancer of breast [RCV000162275]	uncertain significance	15	90966398	90966398	Human	1	name
9850466	CV167500	single nucleotide variant	NM_003981.4(PRC1):c.*919G>T	Familial cancer of breast [RCV000162276]	uncertain significance	15	90966212	90966212	Human	1	name
15162741	CV731029	single nucleotide variant	NM_003981.4(PRC1):c.971-4G>A	not provided [RCV000881818]	benign	15	90979298	90979298	Human		name
9850447	CV167479	single nucleotide variant	NM_003981.4(PRC1):c.145-81A>T	Familial cancer of breast [RCV000162255]	uncertain significance	15	90984221	90984221	Human	1	name
9850457	CV167490	single nucleotide variant	NM_003981.4(PRC1):c.1351-3C>T	Familial cancer of breast [RCV000162266]	uncertain significance	15	90974249	90974249	Human	1	name
9850448	CV167480	single nucleotide variant	NM_003981.4(PRC1):c.12-2765T>C	Familial cancer of breast [RCV000162256]	uncertain significance	15	90987590	90987590	Human	1	name
9850449	CV167482	single nucleotide variant	NM_003981.4(PRC1):c.268-203A>G	Familial cancer of breast [RCV000162258]	uncertain significance	15	90982184	90982184	Human	1	name
9850450	CV167483	single nucleotide variant	NM_003981.4(PRC1):c.268-107G>A	Familial cancer of breast [RCV000162259]	uncertain significance	15	90982088	90982088	Human	5	name
9850450	CV167483	single nucleotide variant	NM_003981.4(PRC1):c.268-107G>A	Familial cancer of breast [RCV000162259]	uncertain significance	15	90982088	90982089	Human	5	name
9850451	CV167484	single nucleotide variant	NM_003981.4(PRC1):c.970+436G>A	Familial cancer of breast [RCV000162260]	uncertain significance	15	90979806	90979806	Human	1	name
9850452	CV167485	single nucleotide variant	NM_003981.4(PRC1):c.971-466T>C	Familial cancer of breast [RCV000162261]	uncertain significance	15	90979760	90979760	Human	1	name
9850453	CV167486	single nucleotide variant	NM_003981.4(PRC1):c.971-442C>T	Breast carcinoma [RCV000162262]	association	15	90979736	90979736	Human	2	name
9850454	CV167487	single nucleotide variant	NM_003981.4(PRC1):c.971-441G>A	Familial cancer of breast [RCV000162263]	uncertain significance	15	90979735	90979735	Human	1	name
9850455	CV167488	single nucleotide variant	NM_003981.4(PRC1):c.971-375A>G	Familial cancer of breast [RCV000162264]	uncertain significance	15	90979669	90979669	Human	1	name
9850456	CV167489	single nucleotide variant	NM_003981.4(PRC1):c.1350+35C>G	Familial cancer of breast [RCV000162265]	uncertain significance	15	90974550	90974550	Human	1	name
9850459	CV167493	single nucleotide variant	NM_003981.4(PRC1):c.1792-828T>C	Familial cancer of breast [RCV000162269]	uncertain significance	15	90968030	90968030	Human	1	name
9850458	CV167491	single nucleotide variant	NM_003981.4(PRC1):c.1462-1016G>A	Breast carcinoma [RCV000162267]	association	15	90971530	90971530	Human	2	name
9850373	CV167481	single nucleotide variant	NM_003981.4(PRC1):c.282G>A (p.Thr94=)	Familial cancer of breast [RCV000162257]	uncertain significance	15	90981967	90981967	Human	1	name
401733153	CV2712992	single nucleotide variant	NM_003981.4(PRC1):c.233C>T (p.Thr78Ile)	not specified [RCV004314698]	uncertain significance	15	90984052	90984052	Human		name
405660269	CV3379052	single nucleotide variant	NM_003981.4(PRC1):c.113A>G (p.Gln38Arg)	not specified [RCV004512684]	uncertain significance	15	90984724	90984724	Human		name
155916636	CV2197525	single nucleotide variant	NM_003981.4(PRC1):c.644T>C (p.Ile215Thr)	not specified [RCV004081249]	uncertain significance	15	90981527	90981527	Human		name
156256621	CV2204522	single nucleotide variant	NM_003981.4(PRC1):c.719G>A (p.Arg240His)	not specified [RCV004081641]	uncertain significance	15	90980987	90980987	Human		name
156333419	CV2220836	single nucleotide variant	NM_003981.4(PRC1):c.667C>T (p.Arg223Trp)	not specified [RCV004092269]	uncertain significance	15	90981504	90981504	Human		name
156237526	CV2235690	single nucleotide variant	NM_003981.4(PRC1):c.613G>A (p.Glu205Lys)	not specified [RCV004111831]	uncertain significance	15	90981558	90981558	Human		name
156077103	CV2291580	single nucleotide variant	NM_003981.4(PRC1):c.440T>C (p.Val147Ala)	not specified [RCV004155880]	uncertain significance	15	90981809	90981809	Human		name
155982114	CV2337127	single nucleotide variant	NM_003981.4(PRC1):c.680T>C (p.Met227Thr)	not specified [RCV004192887]	uncertain significance	15	90981026	90981026	Human		name
156098343	CV2392778	single nucleotide variant	NM_003981.4(PRC1):c.893G>A (p.Arg298Gln)	not specified [RCV004247143]	uncertain significance	15	90980319	90980319	Human		name
329396984	CV2463734	single nucleotide variant	NM_003981.4(PRC1):c.742G>A (p.Asp248Asn)	not specified [RCV004279298]	uncertain significance	15	90980964	90980964	Human		name
401766765	CV2680139	single nucleotide variant	NM_003981.4(PRC1):c.332G>A (p.Arg111Gln)	not specified [RCV004286625]	uncertain significance	15	90981917	90981917	Human		name
401870459	CV2762747	single nucleotide variant	NM_003981.4(PRC1):c.863A>G (p.Gln288Arg)	not specified [RCV004340303]	uncertain significance	15	90980349	90980349	Human		name
401860092	CV2765467	single nucleotide variant	NM_003981.4(PRC1):c.935A>G (p.Gln312Arg)	not specified [RCV004341780]	uncertain significance	15	90980277	90980277	Human		name
405660295	CV3379062	single nucleotide variant	NM_003981.4(PRC1):c.875A>C (p.Lys292Thr)	not specified [RCV004512694]	uncertain significance	15	90980337	90980337	Human		name
405660296	CV3379063	single nucleotide variant	NM_003981.4(PRC1):c.896T>C (p.Val299Ala)	not specified [RCV004512695]	uncertain significance	15	90980316	90980316	Human		name
407530008	CV3468027	single nucleotide variant	NM_003981.4(PRC1):c.712G>A (p.Gly238Arg)	not specified [RCV004656421]	uncertain significance	15	90980994	90980994	Human		name
597747485	CV3584474	single nucleotide variant	NM_003981.4(PRC1):c.497C>G (p.Thr166Arg)	not specified [RCV004845839]	uncertain significance	15	90981752	90981752	Human		name
597747505	CV3584478	single nucleotide variant	NM_003981.4(PRC1):c.693A>C (p.Gln231His)	not specified [RCV004845843]	uncertain significance	15	90981013	90981013	Human		name
597747514	CV3584480	single nucleotide variant	NM_003981.4(PRC1):c.418T>C (p.Tyr140His)	not specified [RCV004845845]	uncertain significance	15	90981831	90981831	Human		name
598202966	CV3908004	single nucleotide variant	NM_003981.4(PRC1):c.391C>G (p.Leu131Val)	not specified [RCV005269300]	uncertain significance	15	90981858	90981858	Human		name
598178955	CV3908005	single nucleotide variant	NM_003981.4(PRC1):c.419A>G (p.Tyr140Cys)	not specified [RCV005264741]	uncertain significance	15	90981830	90981830	Human		name
598178962	CV3908006	single nucleotide variant	NM_003981.4(PRC1):c.394T>C (p.Cys132Arg)	not specified [RCV005264742]	uncertain significance	15	90981855	90981855	Human		name
598178969	CV3908007	single nucleotide variant	NM_003981.4(PRC1):c.947A>G (p.Gln316Arg)	not specified [RCV005264743]	uncertain significance	15	90980265	90980265	Human		name
9850374	CV167492	single nucleotide variant	NM_003981.4(PRC1):c.1532A>G (p.Tyr511Cys)	Familial cancer of breast [RCV000162268]	uncertain significance	15	90970444	90970444	Human	1	name
156098270	CV2207042	single nucleotide variant	NM_003981.4(PRC1):c.1406G>A (p.Arg469Gln)	not specified [RCV004085655]	uncertain significance	15	90974191	90974191	Human		name
155902020	CV2301369	single nucleotide variant	NM_003981.4(PRC1):c.1703G>A (p.Arg568His)	not specified [RCV004160524]	uncertain significance	15	90969493	90969493	Human		name
156113271	CV2349105	single nucleotide variant	NM_003981.4(PRC1):c.1739C>T (p.Ser580Phe)	not specified [RCV004205950]	uncertain significance	15	90969457	90969457	Human		name
156103454	CV2352375	single nucleotide variant	NM_003981.4(PRC1):c.1018C>T (p.Arg340Trp)	not specified [RCV004200842]	uncertain significance	15	90979247	90979247	Human		name
155907232	CV2354388	single nucleotide variant	NM_003981.4(PRC1):c.1507C>T (p.Arg503Trp)	not specified [RCV004200342]	uncertain significance	15	90970469	90970469	Human		name
156197003	CV2367283	single nucleotide variant	NM_003981.4(PRC1):c.1672G>T (p.Gly558Cys)	not specified [RCV004215702]	uncertain significance	15	90969524	90969524	Human		name
329392691	CV2439122	single nucleotide variant	NM_003981.4(PRC1):c.1423C>G (p.Arg475Gly)	not specified [RCV004266409]	uncertain significance	15	90974174	90974174	Human		name
329373451	CV2447254	single nucleotide variant	NM_003981.4(PRC1):c.1034A>G (p.Tyr345Cys)	not specified [RCV004262546]	uncertain significance	15	90979231	90979231	Human		name
329397906	CV2466428	single nucleotide variant	NM_003981.4(PRC1):c.1802C>T (p.Ser601Leu)	not specified [RCV004273985]	uncertain significance	15	90967192	90967192	Human		name
401719211	CV2731248	single nucleotide variant	NM_003981.4(PRC1):c.1543G>A (p.Val515Met)	not specified [RCV004332681]	uncertain significance	15	90970433	90970433	Human		name
401781285	CV2732392	single nucleotide variant	NM_003981.4(PRC1):c.1550G>A (p.Arg517Gln)	not specified [RCV004331502]	uncertain significance	15	90970426	90970426	Human		name
401878117	CV2767047	single nucleotide variant	NM_003981.4(PRC1):c.1657G>A (p.Gly553Ser)	not specified [RCV004347457]	uncertain significance	15	90969539	90969539	Human		name
401885777	CV2783383	single nucleotide variant	NM_003981.4(PRC1):c.1755T>G (p.Asp585Glu)	not specified [RCV004365737]	uncertain significance	15	90969115	90969115	Human		name
401888039	CV2791993	single nucleotide variant	NM_003981.4(PRC1):c.1331A>G (p.Glu444Gly)	not specified [RCV004359410]	uncertain significance	15	90974604	90974604	Human		name
405660270	CV3379053	single nucleotide variant	NM_003981.4(PRC1):c.1266G>A (p.Met422Ile)	not specified [RCV004512685]	uncertain significance	15	90974669	90974669	Human		name
405660274	CV3379054	single nucleotide variant	NM_003981.4(PRC1):c.1318C>G (p.Arg440Gly)	not specified [RCV004512686]	uncertain significance	15	90974617	90974617	Human		name
405660277	CV3379055	single nucleotide variant	NM_003981.4(PRC1):c.1496A>G (p.Asn499Ser)	not specified [RCV004512687]	uncertain significance	15	90970480	90970480	Human		name
405660280	CV3379056	single nucleotide variant	NM_003981.4(PRC1):c.1553T>G (p.Leu518Arg)	not specified [RCV004512688]	uncertain significance	15	90970423	90970423	Human		name
405660283	CV3379057	single nucleotide variant	NM_003981.4(PRC1):c.1559C>T (p.Pro520Leu)	not specified [RCV004512689]	uncertain significance	15	90970417	90970417	Human		name
405660285	CV3379058	single nucleotide variant	NM_003981.4(PRC1):c.1619G>A (p.Gly540Asp)	not specified [RCV004512690]	uncertain significance	15	90969577	90969577	Human		name
405660288	CV3379059	single nucleotide variant	NM_003981.4(PRC1):c.1635C>G (p.Asn545Lys)	not specified [RCV004512691]	uncertain significance	15	90969561	90969561	Human		name
407530007	CV3468023	single nucleotide variant	NM_003981.4(PRC1):c.1235T>C (p.Leu412Ser)	not specified [RCV004656420]	uncertain significance	15	90974700	90974700	Human		name
407464977	CV3468024	single nucleotide variant	NM_003981.4(PRC1):c.1457G>T (p.Arg486Leu)	not specified [RCV004660086]	uncertain significance	15	90974140	90974140	Human		name
407464986	CV3468026	single nucleotide variant	NM_003981.4(PRC1):c.1612C>T (p.Arg538Cys)	not specified [RCV004660088]	uncertain significance	15	90969584	90969584	Human		name
597747495	CV3584476	single nucleotide variant	NM_003981.4(PRC1):c.1117T>C (p.Ser373Pro)	not specified [RCV004845841]	uncertain significance	15	90976762	90976762	Human		name
597747500	CV3584477	single nucleotide variant	NM_003981.4(PRC1):c.1438A>G (p.Asn480Asp)	not specified [RCV004845842]	uncertain significance	15	90974159	90974159	Human		name
597747509	CV3584479	single nucleotide variant	NM_003981.4(PRC1):c.1283T>C (p.Phe428Ser)	not specified [RCV004845844]	uncertain significance	15	90974652	90974652	Human		name
598178944	CV3908002	single nucleotide variant	NM_003981.4(PRC1):c.1327A>C (p.Lys443Gln)	not specified [RCV005264739]	uncertain significance	15	90974608	90974608	Human		name
598178950	CV3908003	single nucleotide variant	NM_003981.4(PRC1):c.1808C>T (p.Ala603Val)	not specified [RCV005264740]	uncertain significance	15	90967186	90967186	Human		name
598178976	CV3908008	single nucleotide variant	NM_003981.4(PRC1):c.1707C>G (p.Asn569Lys)	not specified [RCV005264744]	uncertain significance	15	90969489	90969489	Human		name
8635642	CV90864	single nucleotide variant	NM_003981.3(PRC1):c.1520G>A (p.Gly507Glu)	Malignant melanoma [RCV000070962]	not provided	15	90970456	90970456	Human		name
9850462	CV167496	insertion	NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266	Familial cancer of breast [RCV000162272]	uncertain significance	15	90974369	90974370	Human	1	name

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