Hnrnpl Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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66 records found for search term Hnrnpl

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15170787	CV731276	single nucleotide variant	NM_001533.3(HNRNPL):c.710+10G>C	not provided [RCV000883534]	benign	19	38845640	38845640	Human		name
150521112	CV1290851	single nucleotide variant	NM_001533.3(HNRNPL):c.1355+17G>A	not provided [RCV001732495]	benign	19	38838877	38838877	Human		name
15178797	CV716418	single nucleotide variant	NM_001533.3(HNRNPL):c.82C>A (p.Arg28=)	not provided [RCV000973752]	benign	19	38849885	38849885	Human		name
15160285	CV716419	single nucleotide variant	NM_001533.3(HNRNPL):c.43C>A (p.Arg15=)	not provided [RCV000969870]	benign	19	38849924	38849924	Human		name
401719346	CV2701060	single nucleotide variant	NM_001533.3(HNRNPL):c.19C>T (p.Pro7Ser)	not specified [RCV004309660]	uncertain significance	19	38849948	38849948	Human		name
405791288	CV3266982	single nucleotide variant	NM_001533.3(HNRNPL):c.14T>A (p.Leu5Gln)	not specified [RCV004399805]	uncertain significance	19	38849953	38849953	Human		name
156101565	CV2313494	single nucleotide variant	NM_001533.3(HNRNPL):c.64C>A (p.Pro22Thr)	not specified [RCV004163799]	uncertain significance	19	38849903	38849903	Human		name
155993560	CV2381844	single nucleotide variant	NM_001533.3(HNRNPL):c.53A>G (p.Gln18Arg)	not specified [RCV004232286]	uncertain significance	19	38849914	38849914	Human		name
401775012	CV2713737	single nucleotide variant	NM_001533.3(HNRNPL):c.62A>G (p.Gln21Arg)	not specified [RCV004321087]	uncertain significance	19	38849905	38849905	Human		name
405791296	CV3266985	single nucleotide variant	NM_001533.3(HNRNPL):c.68A>G (p.Asp23Gly)	not specified [RCV004399808]	uncertain significance	19	38849899	38849899	Human		name
405791299	CV3266986	single nucleotide variant	NM_001533.3(HNRNPL):c.91G>A (p.Ala31Thr)	not specified [RCV004399809]	uncertain significance	19	38849876	38849876	Human		name
407527891	CV3433725	single nucleotide variant	NM_001533.3(HNRNPL):c.83G>C (p.Arg28Pro)	not specified [RCV004632942]	uncertain significance	19	38849884	38849884	Human		name
597791603	CV3679462	single nucleotide variant	NM_001533.3(HNRNPL):c.67G>A (p.Asp23Asn)	not specified [RCV004933588]	uncertain significance	19	38849900	38849900	Human		name
15139203	CV741856	single nucleotide variant	NM_001533.3(HNRNPL):c.549G>A (p.Gly183=)	not provided [RCV000899108]	benign	19	38845928	38845928	Human		name
401864163	CV2767522	single nucleotide variant	NM_001533.3(HNRNPL):c.172C>T (p.Pro58Ser)	not specified [RCV004343683]	uncertain significance	19	38849795	38849795	Human		name
401910506	CV2808619	single nucleotide variant	NM_001533.3(HNRNPL):c.1416C>T (p.Cys472=)	not provided [RCV003425138]	likely benign	19	38838538	38838538	Human		name
405791294	CV3266984	single nucleotide variant	NM_001533.3(HNRNPL):c.244G>T (p.Ala82Ser)	not specified [RCV004399807]	uncertain significance	19	38849723	38849723	Human		name
598190941	CV3975497	single nucleotide variant	NM_001533.3(HNRNPL):c.188C>G (p.Thr63Ser)	not specified [RCV005354207]	uncertain significance	19	38849779	38849779	Human		name
156337887	CV2224867	single nucleotide variant	NM_001533.3(HNRNPL):c.623C>T (p.Thr208Met)	not specified [RCV004092959]	uncertain significance	19	38845854	38845854	Human		name
401780553	CV2674077	single nucleotide variant	NM_001533.3(HNRNPL):c.866A>G (p.Asn289Ser)	not specified [RCV004295483]	uncertain significance	19	38843856	38843856	Human		name
401896426	CV2781328	single nucleotide variant	NM_001533.3(HNRNPL):c.539C>G (p.Ser180Cys)	not specified [RCV004352344]	uncertain significance	19	38845938	38845938	Human		name
405791302	CV3266987	single nucleotide variant	NM_001533.3(HNRNPL):c.964G>A (p.Gly322Ser)	not specified [RCV004399810]	uncertain significance	19	38840365	38840365	Human		name
597791598	CV3679460	single nucleotide variant	NM_001533.3(HNRNPL):c.815G>A (p.Arg272His)	not specified [RCV004933586]	uncertain significance	19	38843907	38843907	Human		name
597791612	CV3679465	single nucleotide variant	NM_001533.3(HNRNPL):c.889G>A (p.Gly297Ser)	not specified [RCV004933591]	uncertain significance	19	38840551	38840551	Human		name
155921538	CV2208487	single nucleotide variant	NM_001533.3(HNRNPL):c.1463C>A (p.Pro488Gln)	not specified [RCV004091020]	uncertain significance	19	38838491	38838491	Human		name
156051021	CV2391214	single nucleotide variant	NM_001533.3(HNRNPL):c.1699A>C (p.Met567Leu)	not specified [RCV004237230]	uncertain significance	19	38837396	38837396	Human		name
401753916	CV2719109	single nucleotide variant	NM_001533.3(HNRNPL):c.1017C>G (p.His339Gln)	not specified [RCV004324782]	uncertain significance	19	38840312	38840312	Human		name
401720223	CV2737200	deletion	NM_001533.3(HNRNPL):c.88_106del (p.Gly30fs)	not provided [RCV003314139]	uncertain significance	19	38849861	38849879	Human		name
401891116	CV2778652	single nucleotide variant	NM_001533.3(HNRNPL):c.1682T>C (p.Phe561Ser)	not specified [RCV004344295]	uncertain significance	19	38837413	38837413	Human		name
405791291	CV3266983	single nucleotide variant	NM_001533.3(HNRNPL):c.1564G>A (p.Asp522Asn)	not specified [RCV004399806]	uncertain significance	19	38837645	38837645	Human		name
597791593	CV3679458	single nucleotide variant	NM_001533.3(HNRNPL):c.1141A>G (p.Ser381Gly)	not specified [RCV004933584]	uncertain significance	19	38840188	38840188	Human		name
597791595	CV3679459	single nucleotide variant	NM_001533.3(HNRNPL):c.1135G>T (p.Ala379Ser)	not specified [RCV004933585]	uncertain significance	19	38840194	38840194	Human		name
597791600	CV3679461	single nucleotide variant	NM_001533.3(HNRNPL):c.1448A>G (p.Asn483Ser)	not specified [RCV004933587]	uncertain significance	19	38838506	38838506	Human		name
597791606	CV3679463	single nucleotide variant	NM_001533.3(HNRNPL):c.1696C>G (p.Gln566Glu)	not specified [RCV004933589]	uncertain significance	19	38837399	38837399	Human		name
598190923	CV3975492	single nucleotide variant	NM_001533.3(HNRNPL):c.1766C>T (p.Ser589Phe)	not specified [RCV005354205]	uncertain significance	19	38836726	38836726	Human		name
598248869	CV3975493	single nucleotide variant	NM_001533.3(HNRNPL):c.1380G>A (p.Met460Ile)	not specified [RCV005345506]	uncertain significance	19	38838574	38838574	Human		name
598190932	CV3975494	single nucleotide variant	NM_001533.3(HNRNPL):c.1201A>G (p.Asn401Asp)	not specified [RCV005354206]	uncertain significance	19	38840128	38840128	Human		name
598248877	CV3975495	single nucleotide variant	NM_001533.3(HNRNPL):c.1010C>G (p.Pro337Arg)	not specified [RCV005345507]	uncertain significance	19	38840319	38840319	Human		name
598248884	CV3975496	single nucleotide variant	NM_001533.3(HNRNPL):c.1283A>G (p.Asp428Gly)	not specified [RCV005345508]	uncertain significance	19	38838966	38838966	Human		name
8636810	CV92035	single nucleotide variant	NM_001005335.1(HNRNPL):c.801C>T (p.Phe267=)	Malignant melanoma [RCV000072133]	not provided	19	38840129	38840129	Human		name
329387122	CV2463356	single nucleotide variant	NM_138394.4(HNRNPLL):c.23C>G (p.Pro8Arg)	not specified [RCV004275409]	uncertain significance	2	38602604	38602604	Human		name
329386841	CV2452590	single nucleotide variant	NM_138394.4(HNRNPLL):c.80C>T (p.Thr27Ile)	not specified [RCV004275171]	uncertain significance	2	38602547	38602547	Human		name
405791313	CV3266991	single nucleotide variant	NM_138394.4(HNRNPLL):c.28G>A (p.Glu10Lys)	not specified [RCV004399814]	uncertain significance	2	38602599	38602599	Human		name
597791627	CV3679470	single nucleotide variant	NM_138394.4(HNRNPLL):c.73C>T (p.Leu25Phe)	not specified [RCV004933596]	uncertain significance	2	38602554	38602554	Human		name
329373764	CV2452651	single nucleotide variant	NM_138394.4(HNRNPLL):c.163G>A (p.Gly55Ser)	not specified [RCV004275218]	uncertain significance	2	38602464	38602464	Human		name
401762917	CV2707357	single nucleotide variant	NM_138394.4(HNRNPLL):c.179T>G (p.Phe60Cys)	not specified [RCV004312753]	uncertain significance	2	38602448	38602448	Human		name
405791305	CV3266988	single nucleotide variant	NM_138394.4(HNRNPLL):c.118G>A (p.Glu40Lys)	not specified [RCV004399811]	uncertain significance	2	38602509	38602509	Human		name
405791308	CV3266989	single nucleotide variant	NM_138394.4(HNRNPLL):c.211A>C (p.Lys71Gln)	not specified [RCV004399812]	uncertain significance	2	38591627	38591627	Human		name
405791310	CV3266990	single nucleotide variant	NM_138394.4(HNRNPLL):c.232G>C (p.Val78Leu)	not specified [RCV004399813]	uncertain significance	2	38591606	38591606	Human		name
597791616	CV3679466	single nucleotide variant	NM_138394.4(HNRNPLL):c.137C>T (p.Thr46Met)	not specified [RCV004933592]	uncertain significance	2	38602490	38602490	Human		name
597791630	CV3679471	single nucleotide variant	NM_138394.4(HNRNPLL):c.109G>A (p.Glu37Lys)	not specified [RCV004933597]	uncertain significance	2	38602518	38602518	Human		name
598190947	CV3975498	single nucleotide variant	NM_138394.4(HNRNPLL):c.185A>C (p.Gln62Pro)	not specified [RCV005354208]	uncertain significance	2	38602442	38602442	Human		name
598190957	CV3975499	single nucleotide variant	NM_138394.4(HNRNPLL):c.151G>A (p.Gly51Ser)	not specified [RCV005354209]	uncertain significance	2	38602476	38602476	Human		name
598190972	CV3975501	single nucleotide variant	NM_138394.4(HNRNPLL):c.115G>T (p.Gly39Cys)	not specified [RCV005354211]	uncertain significance	2	38602512	38602512	Human		name
156056250	CV2243281	single nucleotide variant	NM_138394.4(HNRNPLL):c.856T>C (p.Phe286Leu)	not specified [RCV004110160]	uncertain significance	2	38577479	38577479	Human		name
329373997	CV2447528	single nucleotide variant	NM_138394.4(HNRNPLL):c.946G>A (p.Ala316Thr)	not specified [RCV004255889]	uncertain significance	2	38573356	38573356	Human		name
401754236	CV2685206	single nucleotide variant	NM_138394.4(HNRNPLL):c.511C>T (p.Leu171Phe)	not specified [RCV004289762]	uncertain significance	2	38585679	38585679	Human		name
401891798	CV2779447	single nucleotide variant	NM_138394.4(HNRNPLL):c.639A>C (p.Glu213Asp)	not provided [RCV004696527]\|not specified [RCV004351084]	uncertain significance	2	38582162	38582162	Human		name
405791316	CV3266992	single nucleotide variant	NM_138394.4(HNRNPLL):c.737G>A (p.Arg246His)	not specified [RCV004399815]	uncertain significance	2	38581978	38581978	Human		name
597791620	CV3679467	single nucleotide variant	NM_138394.4(HNRNPLL):c.488C>T (p.Ser163Leu)	not specified [RCV004933593]	uncertain significance	2	38585702	38585702	Human		name
597791621	CV3679468	single nucleotide variant	NM_138394.4(HNRNPLL):c.749T>C (p.Ile250Thr)	not specified [RCV004933594]	uncertain significance	2	38581966	38581966	Human		name
597791626	CV3679469	single nucleotide variant	NM_138394.4(HNRNPLL):c.599T>C (p.Ile200Thr)	not specified [RCV004933595]	uncertain significance	2	38583874	38583874	Human		name
156003153	CV2347759	single nucleotide variant	NM_138394.4(HNRNPLL):c.1448T>C (p.Ile483Thr)	not specified [RCV004202724]	uncertain significance	2	38568412	38568412	Human		name
329362766	CV2439228	single nucleotide variant	NM_138394.4(HNRNPLL):c.1449C>G (p.Ile483Met)	not specified [RCV004266497]	uncertain significance	2	38568411	38568411	Human		name
329357893	CV2453801	single nucleotide variant	NM_138394.4(HNRNPLL):c.1107G>T (p.Lys369Asn)	not specified [RCV004271209]	uncertain significance	2	38569911	38569911	Human		name
8625365	CV80488	single nucleotide variant	NM_001142650.1(HNRNPLL):c.1369C>T (p.Pro457Ser)	Malignant melanoma [RCV000060565]	not provided	2	38569165	38569165	Human		name

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