List of variants reported as benign for Renal cell carcinoma

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Total variants: 59

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HGVS	dbSNP	gnomAD frequency
NM_000245.4(MET):c.-207C>G	rs1858830	0.39920
NM_000245.4(MET):c.4092G>A (p.Pro1364=)	rs41737	0.34093
NM_000245.4(MET):c.4017G>A (p.Ala1339=)	rs2023748	0.34017
NM_000245.4(MET):c.3858C>T (p.Asp1286=)	rs41736	0.33828
NM_000245.4(MET):c.1944A>G (p.Gln648=)	rs13223756	0.16754
NM_000245.4(MET):c.534C>T (p.Ser178=)	rs35775721	0.07211
NM_000245.4(MET):c.1131C>T (p.Ile377=)	rs28444388	0.05590
NM_000245.4(MET):c.144G>A (p.Ala48=)	rs11762213	0.03399
NM_000245.4(MET):c.1124A>G (p.Asn375Ser)	rs33917957	0.01723
NM_000245.4(MET):c.2975C>T (p.Thr992Ile)	rs56391007	0.00911
NM_000245.4(MET):c.1085T>C (p.Met362Thr)	rs77523018	0.00742
NM_000245.4(MET):c.390C>T (p.Leu130=)	rs150588908	0.00740
NM_000245.4(MET):c.948A>G (p.Ile316Met)	rs35225896	0.00641
NM_000245.4(MET):c.504G>T (p.Glu168Asp)	rs55985569	0.00420
NM_000245.4(MET):c.2908C>T (p.Arg970Cys)	rs34589476	0.00327
NM_000245.4(MET):c.3522T>C (p.His1174=)	rs146651797	0.00243
NM_000245.4(MET):c.1715G>A (p.Ser572Asn)	rs199771406	0.00188
NM_000245.4(MET):c.2662C>T (p.His888Tyr)	rs115574135	0.00166
NM_000245.4(MET):c.654G>A (p.Arg218=)	rs35284565	0.00153
NM_000245.4(MET):c.2584-9T>C	rs74994656	0.00119
NM_000245.4(MET):c.3549C>T (p.Gly1183=)	rs371165052	0.00074
NM_000245.4(MET):c.798G>A (p.Arg266=)	rs185301166	0.00073
NM_000245.4(MET):c.3523-12C>G	rs186524917	0.00053
NM_000245.4(MET):c.607T>A (p.Ser203Thr)	rs200861145	0.00053
NM_000245.4(MET):c.959C>T (p.Ala320Val)	rs35776110	0.00045
NM_000245.4(MET):c.2715C>T (p.Ser905=)	rs45572835	0.00039
NM_000245.4(MET):c.3810C>T (p.Gly1270=)	rs200865810	0.00039
NM_000245.4(MET):c.3028+11G>T	rs369191825	0.00029
NM_000245.4(MET):c.1191C>T (p.Cys397=)	rs35763409	0.00028
NM_000245.4(MET):c.1966-17T>C	rs555288487	0.00027
NM_000245.4(MET):c.1932C>T (p.His644=)	rs45520237	0.00024
NM_000245.4(MET):c.967A>G (p.Ser323Gly)	rs201467281	0.00024
NM_000245.4(MET):c.4105T>C (p.Leu1369=)	rs45575438	0.00021
NM_000245.4(MET):c.3522+12G>T	rs200624981	0.00019
NM_000245.4(MET):c.1263C>T (p.Thr421=)	rs45499391	0.00016
NM_000245.4(MET):c.4087G>A (p.Ala1363Thr)	rs45578433	0.00016
NM_000245.4(MET):c.110T>C (p.Val37Ala)	rs201315884	0.00009
NM_000245.4(MET):c.789G>A (p.Thr263=)	rs554190225	0.00005
NM_000245.4(MET):c.1132G>A (p.Val378Ile)	rs749738523	0.00004
NM_000245.4(MET):c.1320A>G (p.Thr440=)	rs763726060	0.00004
NM_000245.4(MET):c.2658C>T (p.His886=)	rs748950533	0.00003
NM_000245.4(MET):c.690G>A (p.Thr230=)	rs200138253	0.00003
NM_000245.4(MET):c.1965+14T>C	rs543293293	0.00002
NM_000245.4(MET):c.1701+7A>T	rs749081367	0.00001
NM_000245.4(MET):c.3427C>T (p.Leu1143=)	rs774334135	0.00001
NM_000245.4(MET):c.1114G>A (p.Asp372Asn)	rs773200558
NM_000245.4(MET):c.1311C>G (p.Val437=)
NM_000245.4(MET):c.143C>T (p.Ala48Val)	rs80256822
NM_000245.4(MET):c.1528-13del
NM_000245.4(MET):c.1862+15dup	rs768074029
NM_000245.4(MET):c.1863-5del	rs766900241
NM_000245.4(MET):c.1863-5dup	rs766900241
NM_000245.4(MET):c.2102+20del
NM_000245.4(MET):c.2103-7del	rs761227260
NM_000245.4(MET):c.2103-7dup	rs761227260
NM_000245.4(MET):c.2103-8_2103-7del	rs761227260
NM_000245.4(MET):c.2584-7del	rs587780736
NM_000245.4(MET):c.3387C>A (p.Ile1129=)
NM_000245.4(MET):c.468G>A (p.Ser156=)	rs576502224

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