Rpl7 Variant Search Result - Rat Genome Database

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61 records found for search term Rpl7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407487704	CV3476129	single nucleotide variant	NM_000971.4(RPL7):c.7G>C (p.Gly3Arg)	not specified [RCV004665738]	uncertain significance	8	73293606	73293606	Human		name
405738292	CV3320164	single nucleotide variant	NM_000971.4(RPL7):c.11T>C (p.Val4Ala)	not specified [RCV004451985]	likely benign	8	73293602	73293602	Human		name
598128649	CV3887854	single nucleotide variant	NM_000971.4(RPL7):c.208C>A (p.Arg70=)	not provided [RCV005244028]	likely benign	8	73292321	73292321	Human		name
407487709	CV3476130	single nucleotide variant	NM_000971.4(RPL7):c.44C>T (p.Pro15Leu)	not specified [RCV004665739]	uncertain significance	8	73292768	73292768	Human		name
597709524	CV3594239	single nucleotide variant	NM_000971.4(RPL7):c.40G>A (p.Val14Met)	not specified [RCV004860849]	uncertain significance	8	73292772	73292772	Human		name
156083547	CV2381894	single nucleotide variant	NM_000971.4(RPL7):c.139A>G (p.Arg47Gly)	not specified [RCV004225835]	uncertain significance	8	73292390	73292390	Human		name
155904267	CV2385455	single nucleotide variant	NM_000971.4(RPL7):c.165G>T (p.Lys55Asn)	not specified [RCV004233106]	uncertain significance	8	73292364	73292364	Human		name
329391641	CV2448778	single nucleotide variant	NM_000971.4(RPL7):c.292A>G (p.Ile98Val)	not specified [RCV004261473]	uncertain significance	8	73291909	73291909	Human		name
401773325	CV2709243	single nucleotide variant	NM_000971.4(RPL7):c.168C>G (p.His56Gln)	not specified [RCV004316409]	uncertain significance	8	73292361	73292361	Human		name
401739903	CV2709724	single nucleotide variant	NM_000971.4(RPL7):c.122T>G (p.Met41Arg)	not specified [RCV004320717]	uncertain significance	8	73292690	73292690	Human		name
407513731	CV3476127	single nucleotide variant	NM_000971.4(RPL7):c.245A>G (p.Tyr82Cys)	not specified [RCV004674226]	uncertain significance	8	73292284	73292284	Human		name
407487713	CV3476131	single nucleotide variant	NM_000971.4(RPL7):c.209G>T (p.Arg70Leu)	not specified [RCV004665740]	uncertain significance	8	73292320	73292320	Human		name
597709532	CV3594240	single nucleotide variant	NM_000971.4(RPL7):c.151T>C (p.Tyr51His)	not specified [RCV004860850]	uncertain significance	8	73292378	73292378	Human		name
156147789	CV2212860	single nucleotide variant	NM_000971.4(RPL7):c.730A>C (p.Ile244Leu)	not specified [RCV004091518]	uncertain significance	8	73291061	73291061	Human		name
156103387	CV2260504	single nucleotide variant	NM_000971.4(RPL7):c.380A>G (p.Lys127Arg)	not specified [RCV004123289]	uncertain significance	8	73291821	73291821	Human		name
155906905	CV2279516	single nucleotide variant	NM_000971.4(RPL7):c.302T>C (p.Val101Ala)	not specified [RCV004142034]	uncertain significance	8	73291899	73291899	Human		name
156280352	CV2315972	single nucleotide variant	NM_000971.4(RPL7):c.449T>C (p.Val150Ala)	not specified [RCV004172038]	uncertain significance	8	73291641	73291641	Human		name
407513733	CV3476128	single nucleotide variant	NM_000971.4(RPL7):c.356A>G (p.Asn119Ser)	not specified [RCV004674227]	uncertain significance	8	73291845	73291845	Human		name
597785753	CV3594236	single nucleotide variant	NM_000971.4(RPL7):c.599G>A (p.Arg200His)	not specified [RCV004854835]	uncertain significance	8	73291192	73291192	Human		name
598218485	CV3906378	single nucleotide variant	NM_000971.4(RPL7):c.373C>T (p.Leu125Phe)	not specified [RCV005272361]	uncertain significance	8	73291828	73291828	Human		name
598203797	CV3896532	single nucleotide variant	NM_000972.3(RPL7A):c.626+2T>G	RPL7A-related condition [RCV005356760]	uncertain significance	9	133350729	133350729	Human		name , trait
598218503	CV3902924	single nucleotide variant	NM_000972.3(RPL7A):c.19G>T (p.Ala7Ser)	not specified [RCV005272363]	uncertain significance	9	133348937	133348937	Human		name
597709539	CV3594243	single nucleotide variant	NM_000972.3(RPL7A):c.73A>C (p.Lys25Gln)	not specified [RCV004860851]	uncertain significance	9	133348991	133348991	Human		name
401889770	CV2758459	single nucleotide variant	NM_000972.3(RPL7A):c.202G>A (p.Ala68Thr)	not specified [RCV004335109]	uncertain significance	9	133349628	133349628	Human		name
407487716	CV3476132	single nucleotide variant	NM_000972.3(RPL7A):c.158G>T (p.Arg53Leu)	not specified [RCV004665741]	uncertain significance	9	133349584	133349584	Human		name
597785761	CV3594242	single nucleotide variant	NM_000972.3(RPL7A):c.175C>T (p.Arg59Cys)	not specified [RCV004854837]	uncertain significance	9	133349601	133349601	Human		name
597785772	CV3594245	single nucleotide variant	NM_000972.3(RPL7A):c.155C>T (p.Thr52Ile)	not specified [RCV004854839]	uncertain significance	9	133349581	133349581	Human		name
598218511	CV3902925	single nucleotide variant	NM_000972.3(RPL7A):c.160T>C (p.Phe54Leu)	not specified [RCV005272364]	uncertain significance	9	133349586	133349586	Human		name
598218520	CV3902926	single nucleotide variant	NM_000972.3(RPL7A):c.201A>C (p.Arg67Ser)	not specified [RCV005272365]	uncertain significance	9	133349627	133349627	Human		name
401881769	CV2783951	single nucleotide variant	NM_000972.3(RPL7A):c.398C>A (p.Pro133Gln)	not specified [RCV004362371]	uncertain significance	9	133350035	133350035	Human		name
405738301	CV3320166	single nucleotide variant	NM_000972.3(RPL7A):c.575G>A (p.Arg192His)	not specified [RCV004451987]	uncertain significance	9	133350676	133350676	Human		name
597785757	CV3594241	single nucleotide variant	NM_000972.3(RPL7A):c.647C>T (p.Ala216Val)	not specified [RCV004854836]	uncertain significance	9	133351022	133351022	Human		name
597785767	CV3594244	single nucleotide variant	NM_000972.3(RPL7A):c.688T>A (p.Tyr230Asn)	not specified [RCV004854838]	uncertain significance	9	133351063	133351063	Human		name
598218494	CV3902923	single nucleotide variant	NM_000972.3(RPL7A):c.751G>A (p.Ala251Thr)	not specified [RCV005272362]	uncertain significance	9	133351316	133351316	Human		name
598218527	CV3902927	single nucleotide variant	NM_000972.3(RPL7A):c.772G>A (p.Ala258Thr)	not specified [RCV005272366]	uncertain significance	9	133351337	133351337	Human		name
156224299	CV2395129	single nucleotide variant	NM_001366481.3(RPL7L1):c.65C>T (p.Pro22Leu)	not specified [RCV004236806]	uncertain significance	6	42880884	42880884	Human		name
156113261	CV2212684	single nucleotide variant	NM_001366481.3(RPL7L1):c.197A>G (p.His66Arg)	not specified [RCV004085192]	uncertain significance	6	42883500	42883500	Human		name
156385795	CV2228034	single nucleotide variant	NM_001366481.3(RPL7L1):c.107A>G (p.Lys36Arg)	not specified [RCV004096275]	uncertain significance	6	42880926	42880926	Human		name
156005374	CV2281525	single nucleotide variant	NM_001366481.3(RPL7L1):c.269T>G (p.Leu90Trp)	not specified [RCV004153835]	uncertain significance	6	42883572	42883572	Human		name
156305656	CV2338861	single nucleotide variant	NM_001366481.3(RPL7L1):c.281A>G (p.His94Arg)	not specified [RCV004182413]	uncertain significance	6	42883584	42883584	Human		name
329385563	CV2432183	single nucleotide variant	NM_001366481.3(RPL7L1):c.209G>A (p.Arg70Gln)	not specified [RCV004249325]	uncertain significance	6	42883512	42883512	Human		name
401779745	CV2731995	single nucleotide variant	NM_001366481.3(RPL7L1):c.218G>A (p.Arg73His)	not specified [RCV004333230]	uncertain significance	6	42883521	42883521	Human		name
405738308	CV3320167	single nucleotide variant	NM_001366481.3(RPL7L1):c.130C>T (p.Leu44Phe)	not specified [RCV004451988]	uncertain significance	6	42880949	42880949	Human		name
405738315	CV3320168	single nucleotide variant	NM_001366481.3(RPL7L1):c.217C>T (p.Arg73Cys)	not specified [RCV004451989]	uncertain significance	6	42883520	42883520	Human		name
598218557	CV3902931	single nucleotide variant	NM_001366481.3(RPL7L1):c.124C>A (p.Gln42Lys)	not specified [RCV005272370]	uncertain significance	6	42880943	42880943	Human		name
156047977	CV2315733	single nucleotide variant	NM_001366481.3(RPL7L1):c.443C>T (p.Thr148Ile)	not specified [RCV004169745]	uncertain significance	6	42884744	42884744	Human		name
156345680	CV2356316	single nucleotide variant	NM_001366481.3(RPL7L1):c.307G>A (p.Glu103Lys)	not specified [RCV004206124]	uncertain significance	6	42883610	42883610	Human		name
156199246	CV2362852	single nucleotide variant	NM_001366481.3(RPL7L1):c.358C>T (p.Arg120Cys)	not specified [RCV004208962]	uncertain significance	6	42884659	42884659	Human		name
329390691	CV2440276	single nucleotide variant	NM_001366481.3(RPL7L1):c.359G>A (p.Arg120His)	not specified [RCV004262761]	uncertain significance	6	42884660	42884660	Human		name
329391462	CV2448587	single nucleotide variant	NM_001366481.3(RPL7L1):c.453T>G (p.Phe151Leu)	not specified [RCV004259263]	uncertain significance	6	42885977	42885977	Human		name
329362958	CV2449592	single nucleotide variant	NM_001366481.3(RPL7L1):c.725A>G (p.Tyr242Cys)	not specified [RCV004268517]	uncertain significance	6	42886421	42886421	Human		name
401721854	CV2680708	single nucleotide variant	NM_001366481.3(RPL7L1):c.302G>A (p.Arg101His)	not specified [RCV004291319]	uncertain significance	6	42883605	42883605	Human		name
401888801	CV2764725	single nucleotide variant	NM_001366481.3(RPL7L1):c.536A>G (p.Asn179Ser)	not specified [RCV004334838]	uncertain significance	6	42886060	42886060	Human		name
405738320	CV3320169	single nucleotide variant	NM_001366481.3(RPL7L1):c.304A>G (p.Ile102Val)	not specified [RCV004451990]	uncertain significance	6	42883607	42883607	Human		name
407513736	CV3476133	single nucleotide variant	NM_001366481.3(RPL7L1):c.758A>G (p.Gln253Arg)	not specified [RCV004674228]	uncertain significance	6	42886454	42886454	Human		name
407487721	CV3476134	single nucleotide variant	NM_001366481.3(RPL7L1):c.458A>C (p.Asn153Thr)	not specified [RCV004665742]	uncertain significance	6	42885982	42885982	Human		name
597709549	CV3594246	single nucleotide variant	NM_001366481.3(RPL7L1):c.301C>T (p.Arg101Cys)	not specified [RCV004860852]	uncertain significance	6	42883604	42883604	Human		name
597709558	CV3594247	single nucleotide variant	NM_001366481.3(RPL7L1):c.713G>A (p.Gly238Asp)	not specified [RCV004860853]	uncertain significance	6	42886409	42886409	Human		name
598218535	CV3902928	single nucleotide variant	NM_001366481.3(RPL7L1):c.548A>G (p.Glu183Gly)	not specified [RCV005272367]	uncertain significance	6	42886072	42886072	Human		name
598218549	CV3902930	single nucleotide variant	NM_001366481.3(RPL7L1):c.539C>A (p.Thr180Lys)	not specified [RCV005272369]	uncertain significance	6	42886063	42886063	Human		name
598218565	CV3902932	single nucleotide variant	NM_001366481.3(RPL7L1):c.529A>G (p.Thr177Ala)	not specified [RCV005272371]	uncertain significance	6	42886053	42886053	Human		name

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