Prrg3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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39 records found for search term Prrg3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8628725	CV83869	single nucleotide variant	NM_024082.3(PRRG3):c.115G>T (p.Glu39Ter)	Malignant melanoma [RCV000063950]	not provided	X	151700103	151700103	Human		name
156209728	CV2370152	single nucleotide variant	NM_001372163.1(PRRG3):c.83G>A (p.Arg28His)	not specified [RCV004211036]	uncertain significance	X	151700071	151700071	Human		name
156226150	CV2401077	single nucleotide variant	NM_001372163.1(PRRG3):c.62A>G (p.Asn21Ser)	not specified [RCV004245648]	uncertain significance	X	151700050	151700050	Human		name
401921565	CV2824218	single nucleotide variant	NM_001372163.1(PRRG3):c.672C>T (p.Ala224=)	not provided [RCV003432529]	likely benign	X	151701009	151701009	Human		name
597761682	CV3584830	single nucleotide variant	NM_001372163.1(PRRG3):c.56G>A (p.Arg19His)	not specified [RCV004849183]	uncertain significance	X	151700044	151700044	Human		name
597761708	CV3584836	single nucleotide variant	NM_001372163.1(PRRG3):c.65A>G (p.Glu22Gly)	not specified [RCV004849188]	uncertain significance	X	151700053	151700053	Human		name
401873431	CV2776585	single nucleotide variant	NM_001372163.1(PRRG3):c.101G>A (p.Arg34Gln)	not specified [RCV004355678]	uncertain significance	X	151700089	151700089	Human		name
407531242	CV3461451	single nucleotide variant	NM_001372163.1(PRRG3):c.223C>G (p.Gln75Glu)	not specified [RCV004657493]	uncertain significance	X	151700560	151700560	Human		name
407531244	CV3461452	single nucleotide variant	NM_001372163.1(PRRG3):c.214G>T (p.Asp72Tyr)	not specified [RCV004657494]	uncertain significance	X	151700551	151700551	Human		name
407513919	CV3461455	single nucleotide variant	NM_001372163.1(PRRG3):c.253C>A (p.Pro85Thr)	not specified [RCV004648992]	uncertain significance	X	151700590	151700590	Human		name
597761697	CV3584834	single nucleotide variant	NM_001372163.1(PRRG3):c.224A>G (p.Gln75Arg)	not specified [RCV004849186]	uncertain significance	X	151700561	151700561	Human		name
598161548	CV3901618	single nucleotide variant	NM_001372163.1(PRRG3):c.286G>T (p.Ala96Ser)	not specified [RCV005261071]	uncertain significance	X	151700623	151700623	Human		name
598161543	CV3901619	single nucleotide variant	NM_001372163.1(PRRG3):c.166A>G (p.Thr56Ala)	not specified [RCV005261072]	uncertain significance	X	151700154	151700154	Human		name
156324164	CV2198578	single nucleotide variant	NM_001372163.1(PRRG3):c.487C>T (p.Arg163Trp)	not specified [RCV004075600]	uncertain significance	X	151700824	151700824	Human		name
156227565	CV2199334	single nucleotide variant	NM_001372163.1(PRRG3):c.628G>A (p.Val210Met)	not specified [RCV004070913]	likely benign	X	151700965	151700965	Human		name
156192423	CV2202382	single nucleotide variant	NM_001372163.1(PRRG3):c.370C>T (p.Arg124Cys)	not specified [RCV004080697]	uncertain significance	X	151700707	151700707	Human		name
156038124	CV2218748	single nucleotide variant	NM_001372163.1(PRRG3):c.355C>T (p.Arg119Trp)	not specified [RCV004084668]	uncertain significance	X	151700692	151700692	Human		name
156237028	CV2224177	single nucleotide variant	NM_001372163.1(PRRG3):c.632C>A (p.Ser211Tyr)	not specified [RCV004096025]	uncertain significance	X	151700969	151700969	Human		name
155913688	CV2245929	single nucleotide variant	NM_001372163.1(PRRG3):c.385C>G (p.Leu129Val)	not specified [RCV004113554]	uncertain significance	X	151700722	151700722	Human		name
156368232	CV2266964	single nucleotide variant	NM_001372163.1(PRRG3):c.552A>C (p.Arg184Ser)	not specified [RCV004131616]	uncertain significance	X	151700889	151700889	Human		name
155982251	CV2272946	single nucleotide variant	NM_001372163.1(PRRG3):c.642C>A (p.Asp214Glu)	not specified [RCV004135833]	uncertain significance	X	151700979	151700979	Human		name
156338069	CV2343140	single nucleotide variant	NM_001372163.1(PRRG3):c.673G>A (p.Ala225Thr)	not specified [RCV004194774]	uncertain significance	X	151701010	151701010	Human		name
155998819	CV2396308	single nucleotide variant	NM_001372163.1(PRRG3):c.382A>G (p.Thr128Ala)	not specified [RCV004242040]	uncertain significance	X	151700719	151700719	Human		name
401779131	CV2702221	single nucleotide variant	NM_001372163.1(PRRG3):c.516G>C (p.Glu172Asp)	not specified [RCV004314565]	uncertain significance	X	151700853	151700853	Human		name
401729469	CV2733073	single nucleotide variant	NM_001372163.1(PRRG3):c.491G>A (p.Gly164Glu)	not specified [RCV004332007]	uncertain significance	X	151700828	151700828	Human		name
401868502	CV2767256	single nucleotide variant	NM_001372163.1(PRRG3):c.596C>T (p.Ala199Val)	not specified [RCV004349429]	uncertain significance	X	151700933	151700933	Human		name
401893907	CV2774282	single nucleotide variant	NM_001372163.1(PRRG3):c.446G>A (p.Arg149Gln)	not specified [RCV004347646]	uncertain significance	X	151700783	151700783	Human		name
401867992	CV2791149	single nucleotide variant	NM_001372163.1(PRRG3):c.490G>C (p.Gly164Arg)	not specified [RCV004356512]	uncertain significance	X	151700827	151700827	Human		name
401921564	CV2824217	single nucleotide variant	NM_001372163.1(PRRG3):c.508C>T (p.Arg170Trp)	not provided [RCV003432528]\|not specified [RCV004654218]	likely benign\|uncertain significance	X	151700845	151700845	Human		name
405654137	CV3379177	single nucleotide variant	NM_001372163.1(PRRG3):c.679C>G (p.Pro227Ala)	not specified [RCV004510547]	uncertain significance	X	151701016	151701016	Human		name
405654139	CV3379178	single nucleotide variant	NM_001372163.1(PRRG3):c.680C>G (p.Pro227Arg)	not specified [RCV004510548]	uncertain significance	X	151701017	151701017	Human		name
407513913	CV3461453	single nucleotide variant	NM_001372163.1(PRRG3):c.628G>C (p.Val210Leu)	not specified [RCV004648990]	uncertain significance	X	151700965	151700965	Human		name
597761672	CV3584828	single nucleotide variant	NM_001372163.1(PRRG3):c.329G>A (p.Arg110His)	not specified [RCV004849181]	uncertain significance	X	151700666	151700666	Human		name
597761677	CV3584829	single nucleotide variant	NM_001372163.1(PRRG3):c.554T>G (p.Leu185Arg)	not specified [RCV004849182]	uncertain significance	X	151700891	151700891	Human		name
597761693	CV3584833	single nucleotide variant	NM_001372163.1(PRRG3):c.422G>A (p.Ser141Asn)	not specified [RCV004849185]	uncertain significance	X	151700759	151700759	Human		name
597761704	CV3584835	single nucleotide variant	NM_001372163.1(PRRG3):c.440G>A (p.Gly147Glu)	not specified [RCV004849187]	uncertain significance	X	151700777	151700777	Human		name
598161563	CV3901615	single nucleotide variant	NM_001372163.1(PRRG3):c.610A>C (p.Ser204Arg)	not specified [RCV005261068]	uncertain significance	X	151700947	151700947	Human		name
598161558	CV3901616	single nucleotide variant	NM_001372163.1(PRRG3):c.356G>A (p.Arg119Gln)	not specified [RCV005261069]	uncertain significance	X	151700693	151700693	Human		name
598161553	CV3901617	single nucleotide variant	NM_001372163.1(PRRG3):c.563C>G (p.Thr188Ser)	not specified [RCV005261070]	uncertain significance	X	151700900	151700900	Human		name

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