Rrp1b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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63 records found for search term Rrp1b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15184771	CV778465	single nucleotide variant	NM_015056.3(RRP1B):c.358-8T>A	not provided [RCV000952790]	benign	21	43674628	43674628	Human		name
15180442	CV717233	single nucleotide variant	NM_015056.3(RRP1B):c.246C>T (p.Val82=)	not provided [RCV000974154]	benign	21	43672340	43672340	Human		name
329359558	CV2446323	single nucleotide variant	NM_015056.3(RRP1B):c.86A>G (p.Lys29Arg)	not specified [RCV004249455]	likely benign	21	43659750	43659750	Human		name
8628620	CV83764	single nucleotide variant	NM_015056.2(RRP1B):c.855C>T (p.Asp285=)	Malignant melanoma [RCV000063845]	not provided	21	43683337	43683337	Human		name
150337204	CV1166368	single nucleotide variant	NM_015056.3(RRP1B):c.1557A>G (p.Gln519=)	not provided [RCV001532457]	likely benign	21	43687931	43687931	Human		name
156399899	CV2202293	single nucleotide variant	NM_015056.3(RRP1B):c.142C>G (p.Gln48Glu)	not specified [RCV004078224]	uncertain significance	21	43669895	43669895	Human		name
401920271	CV2824808	single nucleotide variant	NM_015056.3(RRP1B):c.266C>T (p.Ala89Val)	not provided [RCV003431525]\|not specified [RCV004661653]	likely benign\|uncertain significance	21	43672360	43672360	Human		name
156368982	CV2193838	single nucleotide variant	NM_015056.3(RRP1B):c.985A>C (p.Lys329Gln)	not specified [RCV004074586]	uncertain significance	21	43684646	43684646	Human		name
155991786	CV2253387	single nucleotide variant	NM_015056.3(RRP1B):c.400C>G (p.Arg134Gly)	not specified [RCV004125120]	uncertain significance	21	43674678	43674678	Human		name
156178823	CV2298328	single nucleotide variant	NM_015056.3(RRP1B):c.641G>A (p.Arg214Gln)	not specified [RCV004160226]	uncertain significance	21	43676759	43676759	Human		name
155956638	CV2304058	single nucleotide variant	NM_015056.3(RRP1B):c.997G>T (p.Asp333Tyr)	not specified [RCV004170104]	uncertain significance	21	43685777	43685777	Human		name
155961745	CV2311945	single nucleotide variant	NM_015056.3(RRP1B):c.997G>A (p.Asp333Asn)	not specified [RCV004170767]	uncertain significance	21	43685777	43685777	Human		name
156067306	CV2324061	single nucleotide variant	NM_015056.3(RRP1B):c.748C>A (p.Pro250Thr)	not specified [RCV004178357]	uncertain significance	21	43676866	43676866	Human		name
156133725	CV2350394	single nucleotide variant	NM_015056.3(RRP1B):c.772A>G (p.Arg258Gly)	not specified [RCV004202337]	uncertain significance	21	43676890	43676890	Human		name
401770523	CV2685750	single nucleotide variant	NM_015056.3(RRP1B):c.842G>A (p.Arg281Lys)	not specified [RCV004294742]	uncertain significance	21	43683324	43683324	Human		name
401889783	CV2763390	single nucleotide variant	NM_015056.3(RRP1B):c.692C>T (p.Thr231Met)	not specified [RCV004349280]	uncertain significance	21	43676810	43676810	Human		name
405741108	CV3316681	single nucleotide variant	NM_015056.3(RRP1B):c.343G>A (p.Asp115Asn)	not specified [RCV004452392]	uncertain significance	21	43673941	43673941	Human		name
405741124	CV3316683	single nucleotide variant	NM_015056.3(RRP1B):c.968G>A (p.Arg323His)	not specified [RCV004452394]	uncertain significance	21	43684629	43684629	Human		name
407513899	CV3476381	single nucleotide variant	NM_015056.3(RRP1B):c.314A>G (p.Glu105Gly)	not specified [RCV004674289]	uncertain significance	21	43673912	43673912	Human		name
407513906	CV3476385	single nucleotide variant	NM_015056.3(RRP1B):c.785A>G (p.Lys262Arg)	not specified [RCV004674291]	uncertain significance	21	43676903	43676903	Human		name
597786649	CV3604614	single nucleotide variant	NM_015056.3(RRP1B):c.917G>A (p.Arg306Gln)	not specified [RCV004855066]	uncertain significance	21	43684578	43684578	Human		name
598192448	CV3903235	single nucleotide variant	NM_015056.3(RRP1B):c.859G>A (p.Gly287Arg)	not specified [RCV005267140]	uncertain significance	21	43683341	43683341	Human		name
598192458	CV3903237	single nucleotide variant	NM_015056.3(RRP1B):c.520G>A (p.Asp174Asn)	not specified [RCV005267142]	uncertain significance	21	43675134	43675134	Human		name
150337206	CV1166369	single nucleotide variant	NM_015056.3(RRP1B):c.2123C>T (p.Thr708Met)	not provided [RCV001532458]	uncertain significance	21	43693229	43693229	Human		name
156270397	CV2195161	single nucleotide variant	NM_015056.3(RRP1B):c.2029A>G (p.Thr677Ala)	not specified [RCV004080109]	uncertain significance	21	43691448	43691448	Human		name
156062584	CV2203619	single nucleotide variant	NM_015056.3(RRP1B):c.2146G>A (p.Asp716Asn)	not specified [RCV004072807]	likely benign	21	43693252	43693252	Human		name
156401730	CV2217609	single nucleotide variant	NM_015056.3(RRP1B):c.1065C>A (p.Asp355Glu)	not specified [RCV004090131]	uncertain significance	21	43686859	43686859	Human		name
155946619	CV2238150	single nucleotide variant	NM_015056.3(RRP1B):c.1480C>G (p.Pro494Ala)	not specified [RCV004111160]	uncertain significance	21	43687854	43687854	Human		name
156114219	CV2268522	single nucleotide variant	NM_015056.3(RRP1B):c.1918A>G (p.Ser640Gly)	not specified [RCV004130206]	uncertain significance	21	43690339	43690339	Human		name
156064865	CV2272454	single nucleotide variant	NM_015056.3(RRP1B):c.2193C>G (p.Ser731Arg)	not specified [RCV004133372]	uncertain significance	21	43693299	43693299	Human		name
155907194	CV2302166	single nucleotide variant	NM_015056.3(RRP1B):c.1426C>T (p.Arg476Trp)	not specified [RCV004159173]	uncertain significance	21	43687800	43687800	Human		name
156160659	CV2323379	single nucleotide variant	NM_015056.3(RRP1B):c.1549G>A (p.Gly517Arg)	not specified [RCV004171777]	uncertain significance	21	43687923	43687923	Human		name
156292968	CV2336349	single nucleotide variant	NM_015056.3(RRP1B):c.1216A>C (p.Lys406Gln)	not specified [RCV004194572]	uncertain significance	21	43687590	43687590	Human		name
155913122	CV2341714	single nucleotide variant	NM_015056.3(RRP1B):c.2011G>T (p.Ala671Ser)	not specified [RCV004182633]	uncertain significance	21	43690432	43690432	Human		name
156054184	CV2344612	single nucleotide variant	NM_015056.3(RRP1B):c.1843G>A (p.Glu615Lys)	not specified [RCV004197384]	uncertain significance	21	43688217	43688217	Human		name
155939308	CV2376664	single nucleotide variant	NM_015056.3(RRP1B):c.1573C>T (p.Arg525Trp)	not specified [RCV004222861]	uncertain significance	21	43687947	43687947	Human		name
156391807	CV2382623	single nucleotide variant	NM_015056.3(RRP1B):c.1693C>A (p.Pro565Thr)	not specified [RCV004232946]	uncertain significance	21	43688067	43688067	Human		name
156133548	CV2382973	single nucleotide variant	NM_015056.3(RRP1B):c.1951C>G (p.Pro651Ala)	not specified [RCV004217560]	uncertain significance	21	43690372	43690372	Human		name
155970358	CV2392200	single nucleotide variant	NM_015056.3(RRP1B):c.1420C>T (p.Arg474Trp)	not specified [RCV004242542]	uncertain significance	21	43687794	43687794	Human		name
401720773	CV2673483	single nucleotide variant	NM_015056.3(RRP1B):c.1550G>A (p.Gly517Glu)	not specified [RCV004288452]	uncertain significance	21	43687924	43687924	Human		name
401731108	CV2674263	single nucleotide variant	NM_015056.3(RRP1B):c.1994C>T (p.Thr665Ile)	not specified [RCV004289147]	uncertain significance	21	43690415	43690415	Human		name
405741067	CV3316676	single nucleotide variant	NM_015056.3(RRP1B):c.1241C>G (p.Pro414Arg)	not specified [RCV004452387]	uncertain significance	21	43687615	43687615	Human		name
405741075	CV3316677	single nucleotide variant	NM_015056.3(RRP1B):c.1306C>G (p.Leu436Val)	not specified [RCV004452388]	uncertain significance	21	43687680	43687680	Human		name
405741094	CV3316679	single nucleotide variant	NM_015056.3(RRP1B):c.1472T>C (p.Val491Ala)	not specified [RCV004452390]	likely benign	21	43687846	43687846	Human		name
405741101	CV3316680	single nucleotide variant	NM_015056.3(RRP1B):c.1797G>C (p.Met599Ile)	not specified [RCV004452391]	uncertain significance	21	43688171	43688171	Human		name
407467967	CV3476379	single nucleotide variant	NM_015056.3(RRP1B):c.2209C>A (p.Pro737Thr)	not specified [RCV004660953]	uncertain significance	21	43693315	43693315	Human		name
407467969	CV3476380	single nucleotide variant	NM_015056.3(RRP1B):c.1616C>T (p.Thr539Met)	not specified [RCV004660954]	uncertain significance	21	43687990	43687990	Human		name
407467971	CV3476382	single nucleotide variant	NM_015056.3(RRP1B):c.1160T>C (p.Val387Ala)	not specified [RCV004660955]	likely benign	21	43687534	43687534	Human		name
407513902	CV3476383	single nucleotide variant	NM_015056.3(RRP1B):c.1015A>C (p.Ser339Arg)	not specified [RCV004674290]	uncertain significance	21	43686809	43686809	Human		name
407467973	CV3476384	single nucleotide variant	NM_015056.3(RRP1B):c.1403T>C (p.Met468Thr)	not specified [RCV004660956]	likely benign	21	43687777	43687777	Human		name
597710893	CV3604615	single nucleotide variant	NM_015056.3(RRP1B):c.1197A>T (p.Arg399Ser)	not specified [RCV004861013]	uncertain significance	21	43687571	43687571	Human		name
597710901	CV3604616	single nucleotide variant	NM_015056.3(RRP1B):c.1316T>C (p.Leu439Pro)	not specified [RCV004861014]	likely benign	21	43687690	43687690	Human		name
597710921	CV3604618	single nucleotide variant	NM_015056.3(RRP1B):c.1016G>A (p.Ser339Asn)	not specified [RCV004861016]	uncertain significance	21	43686810	43686810	Human		name
597710931	CV3604619	single nucleotide variant	NM_015056.3(RRP1B):c.1027C>G (p.Leu343Val)	not specified [RCV004861017]	uncertain significance	21	43686821	43686821	Human		name
597710940	CV3604620	single nucleotide variant	NM_015056.3(RRP1B):c.1797G>A (p.Met599Ile)	not specified [RCV004861018]	uncertain significance	21	43688171	43688171	Human		name
598192400	CV3903228	single nucleotide variant	NM_015056.3(RRP1B):c.1381G>A (p.Glu461Lys)	not specified [RCV005267133]	uncertain significance	21	43687755	43687755	Human		name
598192409	CV3903229	single nucleotide variant	NM_015056.3(RRP1B):c.1325G>A (p.Arg442His)	not specified [RCV005267134]	uncertain significance	21	43687699	43687699	Human		name
598192422	CV3903231	single nucleotide variant	NM_015056.3(RRP1B):c.1658G>A (p.Gly553Asp)	not specified [RCV005267136]	uncertain significance	21	43688032	43688032	Human		name
598192429	CV3903232	single nucleotide variant	NM_015056.3(RRP1B):c.1927G>T (p.Val643Leu)	not specified [RCV005267137]	uncertain significance	21	43690348	43690348	Human		name
598192437	CV3903233	single nucleotide variant	NM_015056.3(RRP1B):c.1477C>A (p.Pro493Thr)	not specified [RCV005267138]	uncertain significance	21	43687851	43687851	Human		name
598192444	CV3903234	single nucleotide variant	NM_015056.3(RRP1B):c.1676A>G (p.Asn559Ser)	not specified [RCV005267139]	uncertain significance	21	43688050	43688050	Human		name
598192453	CV3903236	single nucleotide variant	NM_015056.3(RRP1B):c.1484A>T (p.Glu495Val)	not specified [RCV005267141]	uncertain significance	21	43687858	43687858	Human		name
15184773	CV705723	single nucleotide variant	NM_015056.3(RRP1B):c.1892T>C (p.Leu631Pro)	not provided [RCV000952791]	benign	21	43690313	43690313	Human		name

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