Pglyrp3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Pglyrp3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15150707	CV743685	single nucleotide variant	NM_052891.3(PGLYRP3):c.55+9T>C	not provided [RCV000901212]	benign	1	153310602	153310602	Human		name
153301095	CV1688940	single nucleotide variant	NM_052891.3(PGLYRP3):c.258-173T>C	PGLYRP3-associated inflamatory bowel disease [RCV002266668]	uncertain significance	1	153305238	153305238	Human		name , trait
597677432	CV3572114	single nucleotide variant	NM_052891.3(PGLYRP3):c.14C>A (p.Pro5Gln)	not specified [RCV004836835]	uncertain significance	1	153310652	153310652	Human		name
15154036	CV731740	single nucleotide variant	NM_052891.3(PGLYRP3):c.135C>G (p.Ala45=)	not provided [RCV000901877]	benign	1	153307188	153307188	Human		name
401721245	CV2673650	single nucleotide variant	NM_052891.3(PGLYRP3):c.50C>T (p.Ala17Val)	not specified [RCV004282384]	uncertain significance	1	153310616	153310616	Human		name
401768856	CV2686400	single nucleotide variant	NM_052891.3(PGLYRP3):c.89G>A (p.Gly30Glu)	not specified [RCV004297470]	uncertain significance	1	153307234	153307234	Human		name
405748646	CV3364917	single nucleotide variant	NM_052891.3(PGLYRP3):c.34A>C (p.Ile12Leu)	not specified [RCV004498693]	uncertain significance	1	153310632	153310632	Human		name
405747968	CV3364924	single nucleotide variant	NM_052891.3(PGLYRP3):c.86G>C (p.Trp29Ser)	not specified [RCV004498700]	uncertain significance	1	153307237	153307237	Human		name
597766806	CV3572117	single nucleotide variant	NM_052891.3(PGLYRP3):c.43C>T (p.Leu15Phe)	not specified [RCV004850341]	uncertain significance	1	153310623	153310623	Human		name
15194954	CV696116	single nucleotide variant	NM_052891.3(PGLYRP3):c.798T>C (p.Tyr266=)	not provided [RCV000955787]	benign	1	153299162	153299162	Human		name
15187120	CV718239	single nucleotide variant	NM_052891.3(PGLYRP3):c.507A>G (p.Gln169=)	not provided [RCV000887166]	benign	1	153303879	153303879	Human		name
8624703	CV79817	single nucleotide variant	NM_052891.2(PGLYRP3):c.579C>T (p.His193=)	Malignant melanoma [RCV000059893]	not provided	1	153302558	153302558	Human		name
156071975	CV2337791	single nucleotide variant	NM_052891.3(PGLYRP3):c.250G>C (p.Ala84Pro)	not specified [RCV004183808]	uncertain significance	1	153307073	153307073	Human		name
401723359	CV2674924	single nucleotide variant	NM_052891.3(PGLYRP3):c.195G>C (p.Gln65His)	not specified [RCV004296237]	uncertain significance	1	153307128	153307128	Human		name
401758388	CV2694078	single nucleotide variant	NM_052891.3(PGLYRP3):c.233T>C (p.Ile78Thr)	not specified [RCV004302512]	uncertain significance	1	153307090	153307090	Human		name
405748664	CV3364914	single nucleotide variant	NM_052891.3(PGLYRP3):c.191G>A (p.Ser64Asn)	not specified [RCV004498690]	likely benign	1	153307132	153307132	Human		name
405748660	CV3364915	single nucleotide variant	NM_052891.3(PGLYRP3):c.206G>C (p.Gly69Ala)	not specified [RCV004498691]	uncertain significance	1	153307117	153307117	Human		name
405748654	CV3364916	single nucleotide variant	NM_052891.3(PGLYRP3):c.214T>C (p.Ser72Pro)	not specified [RCV004498692]	uncertain significance	1	153307109	153307109	Human		name
407464351	CV3466929	single nucleotide variant	NM_052891.3(PGLYRP3):c.205G>A (p.Gly69Arg)	not specified [RCV004659929]	uncertain significance	1	153307118	153307118	Human		name
597766802	CV3572116	single nucleotide variant	NM_052891.3(PGLYRP3):c.241T>C (p.Cys81Arg)	not specified [RCV004850340]	uncertain significance	1	153307082	153307082	Human		name
15155473	CV696117	single nucleotide variant	NM_052891.3(PGLYRP3):c.202C>T (p.Arg68Trp)	not provided [RCV000946498]	benign	1	153307121	153307121	Human		name
155920620	CV2210852	single nucleotide variant	NM_052891.3(PGLYRP3):c.997A>C (p.Ile333Leu)	not specified [RCV004085939]	uncertain significance	1	153297985	153297985	Human		name
155973054	CV2214417	single nucleotide variant	NM_052891.3(PGLYRP3):c.923C>T (p.Thr308Ile)	not specified [RCV004088177]	uncertain significance	1	153298059	153298059	Human		name
156041849	CV2219604	single nucleotide variant	NM_052891.3(PGLYRP3):c.731T>A (p.Phe244Tyr)	not specified [RCV004095328]	uncertain significance	1	153299229	153299229	Human		name
156054539	CV2243098	single nucleotide variant	NM_052891.3(PGLYRP3):c.746A>T (p.Asp249Val)	not specified [RCV004110009]	uncertain significance	1	153299214	153299214	Human		name
156265006	CV2312167	single nucleotide variant	NM_052891.3(PGLYRP3):c.551G>A (p.Arg184Gln)	not specified [RCV004165070]	uncertain significance	1	153302586	153302586	Human		name
156036252	CV2373971	single nucleotide variant	NM_052891.3(PGLYRP3):c.838T>G (p.Tyr280Asp)	not specified [RCV004227103]	uncertain significance	1	153299122	153299122	Human		name
155966438	CV2396074	single nucleotide variant	NM_052891.3(PGLYRP3):c.356C>A (p.Ala119Asp)	not specified [RCV004237608]	uncertain significance	1	153304967	153304967	Human		name
401719147	CV2679432	single nucleotide variant	NM_052891.3(PGLYRP3):c.457A>G (p.Arg153Gly)	not specified [RCV004285958]	uncertain significance	1	153303929	153303929	Human		name
401767233	CV2681548	single nucleotide variant	NM_052891.3(PGLYRP3):c.704G>A (p.Arg235Gln)	not specified [RCV004292076]	uncertain significance	1	153302433	153302433	Human		name
401750693	CV2700038	single nucleotide variant	NM_052891.3(PGLYRP3):c.347T>C (p.Leu116Pro)	not specified [RCV004310462]	uncertain significance	1	153304976	153304976	Human		name
405748640	CV3364918	single nucleotide variant	NM_052891.3(PGLYRP3):c.427T>C (p.Tyr143His)	not specified [RCV004498694]	uncertain significance	1	153303959	153303959	Human		name
405748432	CV3364919	single nucleotide variant	NM_052891.3(PGLYRP3):c.663G>C (p.Gln221His)	not specified [RCV004498695]	uncertain significance	1	153302474	153302474	Human		name
405748072	CV3364921	single nucleotide variant	NM_052891.3(PGLYRP3):c.719T>C (p.Ile240Thr)	not specified [RCV004498697]	uncertain significance	1	153302418	153302418	Human		name
405747954	CV3364922	single nucleotide variant	NM_052891.3(PGLYRP3):c.740G>A (p.Gly247Asp)	not specified [RCV004498698]	uncertain significance	1	153299220	153299220	Human		name
405747960	CV3364923	single nucleotide variant	NM_052891.3(PGLYRP3):c.857C>T (p.Pro286Leu)	not specified [RCV004498699]	uncertain significance	1	153298125	153298125	Human		name
405747973	CV3364925	single nucleotide variant	NM_052891.3(PGLYRP3):c.967C>G (p.Leu323Val)	not specified [RCV004498701]	uncertain significance	1	153298015	153298015	Human		name
407464355	CV3466930	single nucleotide variant	NM_052891.3(PGLYRP3):c.800G>A (p.Gly267Glu)	not specified [RCV004659930]	uncertain significance	1	153299160	153299160	Human		name
407529003	CV3466931	single nucleotide variant	NM_052891.3(PGLYRP3):c.452C>T (p.Ser151Leu)	not specified [RCV004655824]	uncertain significance	1	153303934	153303934	Human		name
407529005	CV3466932	single nucleotide variant	NM_052891.3(PGLYRP3):c.461A>T (p.Tyr154Phe)	not specified [RCV004655825]	uncertain significance	1	153303925	153303925	Human		name
407464359	CV3466933	single nucleotide variant	NM_052891.3(PGLYRP3):c.385C>T (p.Pro129Ser)	not specified [RCV004659931]	uncertain significance	1	153304001	153304001	Human		name
598247445	CV3999886	single nucleotide variant	NM_052891.3(PGLYRP3):c.678C>A (p.Asn226Lys)	not specified [RCV005384178]	uncertain significance	1	153302459	153302459	Human		name
15102348	CV718238	single nucleotide variant	NM_052891.3(PGLYRP3):c.878C>T (p.Ala293Val)	not provided [RCV000892461]	benign	1	153298104	153298104	Human		name

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