Lbp Variant Search Result - Rat Genome Database

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69 records found for search term Lbp

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405815316	CV3283713	single nucleotide variant	NM_004139.5(LBP):c.20C>T (p.Ala7Val)	not specified [RCV004410301]	uncertain significance	20	38346536	38346536	Human		name
405815317	CV3283714	single nucleotide variant	NM_004139.5(LBP):c.240C>T (p.Ser80=)	not specified [RCV004410302]	likely benign	20	38350811	38350811	Human		name
15163279	CV705475	single nucleotide variant	NM_004139.5(LBP):c.144A>G (p.Leu48=)	not provided [RCV000948048]	benign	20	38349567	38349567	Human	1	name
15163279	CV705475	single nucleotide variant	NM_004139.5(LBP):c.144A>G (p.Leu48=)	not provided [RCV000948048]	benign	20	38349567	38349568	Human	1	name
15193262	CV742398	single nucleotide variant	NM_004139.5(LBP):c.276G>A (p.Ala92=)	not provided [RCV000910789]	likely benign	20	38350847	38350847	Human		name
156387011	CV2364912	single nucleotide variant	NM_004139.5(LBP):c.94G>A (p.Ala32Thr)	not specified [RCV004221812]	uncertain significance	20	38346610	38346610	Human		name
407491078	CV3452445	single nucleotide variant	NM_004139.5(LBP):c.82C>G (p.Pro28Ala)	not specified [RCV004642137]	uncertain significance	20	38346598	38346598	Human		name
407460433	CV3452451	single nucleotide variant	NM_004139.5(LBP):c.59C>T (p.Thr20Ile)	not specified [RCV004633890]	uncertain significance	20	38346575	38346575	Human		name
407491147	CV3452454	single nucleotide variant	NM_004139.5(LBP):c.49C>A (p.Leu17Ile)	not specified [RCV004642144]	uncertain significance	20	38346565	38346565	Human		name
15165043	CV705477	single nucleotide variant	NM_004139.5(LBP):c.612A>G (p.Ser204=)	not provided [RCV000948494]	benign	20	38360727	38360727	Human		name
401762535	CV2696158	single nucleotide variant	NM_004139.5(LBP):c.231G>C (p.Glu77Asp)	not specified [RCV004310215]	uncertain significance	20	38349654	38349654	Human		name
401865184	CV2791546	single nucleotide variant	NM_004139.5(LBP):c.224G>T (p.Arg75Leu)	not specified [RCV004358920]	uncertain significance	20	38349647	38349647	Human		name
401919722	CV2824404	single nucleotide variant	NM_004139.5(LBP):c.1203C>T (p.Phe401=)	not provided [RCV003431319]	likely benign	20	38370791	38370791	Human		name
405815318	CV3283715	single nucleotide variant	NM_004139.5(LBP):c.241C>G (p.Leu81Val)	not specified [RCV004410303]	uncertain significance	20	38350812	38350812	Human		name
407491085	CV3452447	single nucleotide variant	NM_004139.5(LBP):c.214G>A (p.Gly72Ser)	not specified [RCV004642139]	uncertain significance	20	38349637	38349637	Human		name
407491143	CV3452453	single nucleotide variant	NM_004139.5(LBP):c.214G>T (p.Gly72Cys)	not specified [RCV004642143]	uncertain significance	20	38349637	38349637	Human		name
598229637	CV3987764	single nucleotide variant	NM_004139.5(LBP):c.282G>T (p.Arg94Ser)	not specified [RCV005362575]	uncertain significance	20	38350853	38350853	Human		name
15160103	CV716966	single nucleotide variant	NM_004139.5(LBP):c.271T>A (p.Ser91Thr)	not provided [RCV000969834]	likely benign	20	38350842	38350842	Human		name
15099203	CV757515	single nucleotide variant	NM_004139.5(LBP):c.1335C>T (p.Ala445=)	not provided [RCV000914413]	benign	20	38373947	38373947	Human		name
9586902	CV165520	single nucleotide variant	NM_004139.5(LBP):c.998C>T (p.Pro333Leu)	not provided [RCV000143861]	uncertain significance	20	38369011	38369011	Human	19	name
9586902	CV165520	single nucleotide variant	NM_004139.5(LBP):c.998C>T (p.Pro333Leu)	not provided [RCV000143861]	uncertain significance	20	38369011	38369012	Human	19	name
156062277	CV2263198	single nucleotide variant	NM_004139.5(LBP):c.935C>T (p.Ser312Phe)	not specified [RCV004131427]	uncertain significance	20	38366782	38366782	Human		name
155911657	CV2313362	single nucleotide variant	NM_004139.5(LBP):c.893A>G (p.Tyr298Cys)	not specified [RCV004163689]	uncertain significance	20	38364724	38364724	Human		name
155972555	CV2335812	single nucleotide variant	NM_004139.5(LBP):c.676G>A (p.Ala226Thr)	not specified [RCV004196047]	uncertain significance	20	38363998	38363998	Human		name
329398877	CV2443047	single nucleotide variant	NM_004139.5(LBP):c.926C>T (p.Pro309Leu)	not specified [RCV004253635]	uncertain significance	20	38366773	38366773	Human		name
329359146	CV2450891	single nucleotide variant	NM_004139.5(LBP):c.683T>C (p.Ile228Thr)	not specified [RCV004267796]	uncertain significance	20	38364005	38364005	Human		name
401758893	CV2694332	single nucleotide variant	NM_004139.5(LBP):c.659C>T (p.Thr220Ile)	not specified [RCV004304525]	uncertain significance	20	38363981	38363981	Human		name
401772798	CV2712911	single nucleotide variant	NM_004139.5(LBP):c.338A>G (p.Gln113Arg)	not specified [RCV004314312]	uncertain significance	20	38350909	38350909	Human		name
401893464	CV2765320	single nucleotide variant	NM_004139.5(LBP):c.941T>G (p.Ile314Ser)	not specified [RCV004339833]	uncertain significance	20	38366788	38366788	Human		name
405815319	CV3283716	single nucleotide variant	NM_004139.5(LBP):c.367T>C (p.Phe123Leu)	not specified [RCV004410304]	likely benign	20	38350938	38350938	Human		name
405815320	CV3283717	single nucleotide variant	NM_004139.5(LBP):c.448G>A (p.Gly150Arg)	not specified [RCV004410305]	uncertain significance	20	38354363	38354363	Human		name
405815321	CV3283718	single nucleotide variant	NM_004139.5(LBP):c.502G>A (p.Val168Met)	not specified [RCV004410306]	uncertain significance	20	38354417	38354417	Human		name
405815323	CV3283720	single nucleotide variant	NM_004139.5(LBP):c.523G>C (p.Gly175Arg)	not specified [RCV004410308]	uncertain significance	20	38354438	38354438	Human		name
405815324	CV3283721	single nucleotide variant	NM_004139.5(LBP):c.769C>T (p.Arg257Cys)	not specified [RCV004410309]	uncertain significance	20	38364600	38364600	Human		name
405815325	CV3283722	single nucleotide variant	NM_004139.5(LBP):c.776C>T (p.Pro259Leu)	not specified [RCV004410310]	uncertain significance	20	38364607	38364607	Human		name
405815326	CV3283723	single nucleotide variant	NM_004139.5(LBP):c.822C>A (p.Asn274Lys)	not specified [RCV004410311]	uncertain significance	20	38364653	38364653	Human		name
405815327	CV3283724	single nucleotide variant	NM_004139.5(LBP):c.845C>T (p.Ser282Leu)	not specified [RCV004410312]	uncertain significance	20	38364676	38364676	Human		name
407491088	CV3452448	single nucleotide variant	NM_004139.5(LBP):c.968C>A (p.Pro323His)	not specified [RCV004642140]	uncertain significance	20	38366815	38366815	Human		name
407460429	CV3452450	single nucleotide variant	NM_004139.5(LBP):c.979C>T (p.Arg327Trp)	not specified [RCV004633889]	uncertain significance	20	38366826	38366826	Human		name
407491140	CV3452452	single nucleotide variant	NM_004139.5(LBP):c.829G>T (p.Val277Phe)	not specified [RCV004642142]	uncertain significance	20	38364660	38364660	Human		name
597631812	CV3698648	single nucleotide variant	NM_004139.5(LBP):c.501G>T (p.Glu167Asp)	not specified [RCV004939866]	likely benign	20	38354416	38354416	Human		name
597631819	CV3698649	single nucleotide variant	NM_004139.5(LBP):c.452G>A (p.Arg151Lys)	not specified [RCV004939867]	uncertain significance	20	38354367	38354367	Human		name
597631823	CV3698650	single nucleotide variant	NM_004139.5(LBP):c.331C>T (p.Arg111Trp)	not specified [RCV004939868]	uncertain significance	20	38350902	38350902	Human		name
597631826	CV3698651	single nucleotide variant	NM_004139.5(LBP):c.552G>T (p.Gln184His)	not specified [RCV004939869]	uncertain significance	20	38355373	38355373	Human		name
597631830	CV3698652	single nucleotide variant	NM_004139.5(LBP):c.665T>C (p.Ile222Thr)	not specified [RCV004939870]	uncertain significance	20	38363987	38363987	Human		name
598174897	CV3987760	single nucleotide variant	NM_004139.5(LBP):c.319G>A (p.Asp107Asn)	not specified [RCV005371188]	uncertain significance	20	38350890	38350890	Human		name
598174901	CV3987762	single nucleotide variant	NM_004139.5(LBP):c.356G>A (p.Arg119His)	not specified [RCV005371189]	uncertain significance	20	38350927	38350927	Human		name
598174908	CV3987765	single nucleotide variant	NM_004139.5(LBP):c.697G>T (p.Val233Leu)	not specified [RCV005371190]	uncertain significance	20	38364019	38364019	Human		name
598197977	CV3987766	single nucleotide variant	NM_004139.5(LBP):c.839C>A (p.Ala280Asp)	not specified [RCV005355429]	uncertain significance	20	38364670	38364670	Human		name
598197986	CV3987767	single nucleotide variant	NM_004139.5(LBP):c.761G>T (p.Arg254Leu)	not specified [RCV005355430]	uncertain significance	20	38364592	38364592	Human		name
15176596	CV705476	single nucleotide variant	NM_004139.5(LBP):c.373C>A (p.Leu125Ile)	not provided [RCV000950860]	benign	20	38354288	38354288	Human		name
15178731	CV705478	single nucleotide variant	NM_004139.5(LBP):c.622G>A (p.Asp208Asn)	not provided [RCV000951350]	benign	20	38360737	38360737	Human		name
15180409	CV716967	single nucleotide variant	NM_004139.5(LBP):c.726G>A (p.Met242Ile)	not provided [RCV000974144]	likely benign	20	38364048	38364048	Human		name
15152718	CV716968	single nucleotide variant	NM_004139.5(LBP):c.746G>A (p.Gly249Asp)	not provided [RCV000968407]	benign	20	38364577	38364577	Human		name
15098664	CV728647	single nucleotide variant	NM_004139.5(LBP):c.641A>G (p.Gln214Arg)	not provided [RCV000891789]	likely benign	20	38360756	38360756	Human		name
8637302	CV92528	single nucleotide variant	NM_004139.4(LBP):c.959C>T (p.Ser320Phe)	Malignant melanoma [RCV000072626]	not provided	20	38366806	38366806	Human		name
156359843	CV2328316	single nucleotide variant	NM_004139.5(LBP):c.1105C>T (p.Leu369Phe)	not specified [RCV004175434]	uncertain significance	20	38369118	38369118	Human		name
329359125	CV2450855	single nucleotide variant	NM_004139.5(LBP):c.1229A>G (p.Glu410Gly)	not specified [RCV004267767]	uncertain significance	20	38371291	38371291	Human		name
329357213	CV2457588	single nucleotide variant	NM_004139.5(LBP):c.1382T>C (p.Leu461Pro)	not specified [RCV004269172]	likely benign	20	38373994	38373994	Human		name
401754137	CV2685175	single nucleotide variant	NM_004139.5(LBP):c.1209G>C (p.Lys403Asn)	not specified [RCV004289736]	uncertain significance	20	38370797	38370797	Human		name
405815311	CV3283708	single nucleotide variant	NM_004139.5(LBP):c.1231C>G (p.Leu411Val)	not specified [RCV004410296]	uncertain significance	20	38371293	38371293	Human		name
405815312	CV3283709	single nucleotide variant	NM_004139.5(LBP):c.1257C>A (p.Phe419Leu)	not specified [RCV004410297]	uncertain significance	20	38371319	38371319	Human		name
405815313	CV3283710	single nucleotide variant	NM_004139.5(LBP):c.1336G>A (p.Glu446Lys)	not specified [RCV004410298]	likely benign	20	38373948	38373948	Human		name
405815314	CV3283711	single nucleotide variant	NM_004139.5(LBP):c.1397A>G (p.His466Arg)	not specified [RCV004410299]	uncertain significance	20	38374009	38374009	Human		name
405815315	CV3283712	single nucleotide variant	NM_004139.5(LBP):c.1436T>G (p.Met479Arg)	not specified [RCV004410300]	uncertain significance	20	38376659	38376659	Human		name
407491092	CV3452449	single nucleotide variant	NM_004139.5(LBP):c.1186A>G (p.Ser396Gly)	not specified [RCV004642141]	uncertain significance	20	38370774	38370774	Human		name
598197968	CV3987763	single nucleotide variant	NM_004139.5(LBP):c.1403A>G (p.Asp468Gly)	not specified [RCV005355428]	uncertain significance	20	38376626	38376626	Human		name
15140133	CV716969	single nucleotide variant	NM_004139.5(LBP):c.1316A>C (p.Lys439Thr)	not provided [RCV000966087]	benign	20	38373127	38373127	Human		name
15153006	CV728648	single nucleotide variant	NM_004139.5(LBP):c.1015C>T (p.Leu339Phe)	not provided [RCV000879923]	likely benign	20	38369028	38369028	Human		name

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