ClinVar Miner

List of variants in gene RIMS1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_014989.7(RIMS1):c.1083A>G (p.Leu361=) rs2463730 0.97497
NM_014989.7(RIMS1):c.666A>G (p.Leu222=) rs2249021 0.68629
NM_014989.7(RIMS1):c.2928-80C>T rs6923891 0.64993
NM_014989.7(RIMS1):c.1857+61C>T rs2807519 0.64829
NM_014989.7(RIMS1):c.812+93G>A rs17725666 0.28373
NM_014989.7(RIMS1):c.1209G>A (p.Ala403=) rs114505309 0.27986
NM_014989.7(RIMS1):c.4548C>T (p.Phe1516=) rs2815738 0.20033
NM_014989.7(RIMS1):c.460-37C>T rs41265489 0.06803
NM_014989.7(RIMS1):c.3482+79A>T rs6925880 0.05401
NM_014989.7(RIMS1):c.3555-91G>A rs76570730 0.03149
NM_014989.7(RIMS1):c.3470C>T (p.Pro1157Leu) rs41265501 0.02304
NM_014989.7(RIMS1):c.3053+74A>T rs9442761 0.02076
NM_014989.7(RIMS1):c.1679-20565G>A rs9446600 0.02013
NM_014989.7(RIMS1):c.1776G>A (p.Glu592=) rs77121218 0.01826
NM_014989.7(RIMS1):c.743C>T (p.Ser248Leu) rs116476753 0.01524
NM_014989.7(RIMS1):c.648G>A (p.Ser216=) rs116303981 0.00829
NM_014989.7(RIMS1):c.2895G>A (p.Pro965=) rs41265493 0.00819
NM_014989.7(RIMS1):c.2670T>C (p.His890=) rs34821160 0.00550
NM_014989.7(RIMS1):c.5076A>G (p.Ser1692=) rs61736795 0.00409
NM_014989.7(RIMS1):c.1459G>A (p.Ala487Thr) rs200422266 0.00320
NM_014989.7(RIMS1):c.438C>T (p.Arg146=) rs142196418 0.00298
NM_014989.7(RIMS1):c.4923C>T (p.Ile1641=) rs144188801 0.00249
NM_014989.7(RIMS1):c.4983G>A (p.Pro1661=) rs377743730 0.00237
NM_014989.7(RIMS1):c.3308+12T>G rs115294253 0.00192
NM_014989.7(RIMS1):c.3171C>T (p.Ser1057=) rs201355521 0.00174
NM_014989.7(RIMS1):c.2082-9T>C rs199746605 0.00152
NM_014989.7(RIMS1):c.594A>G (p.Thr198=) rs149442461 0.00147
NM_014989.7(RIMS1):c.2699-8T>C rs149883454 0.00100
NM_014989.7(RIMS1):c.1764A>G (p.Gln588=) rs192179523 0.00088
NM_014989.7(RIMS1):c.3471G>A (p.Pro1157=) rs374938269 0.00086
NM_014989.7(RIMS1):c.813-14T>G rs180682682 0.00058
NM_014989.7(RIMS1):c.3117-7G>A rs202107254 0.00032
NM_014989.7(RIMS1):c.2523A>G (p.Glu841=) rs186078277 0.00029
NM_014989.7(RIMS1):c.942G>A (p.Arg314=) rs185069362 0.00025
NM_014989.7(RIMS1):c.812+13T>A rs575748980 0.00019
NM_014989.7(RIMS1):c.3941T>C (p.Leu1314Pro) rs201798320 0.00018
NM_014989.7(RIMS1):c.3194+9C>A rs564292772 0.00017
NM_014989.7(RIMS1):c.3399-4A>G rs368216570 0.00017
NM_014989.7(RIMS1):c.2242-12C>T rs190023733 0.00014
NM_014989.7(RIMS1):c.165-5C>G rs532652925 0.00013
NM_014989.7(RIMS1):c.4860+15G>A rs553488575 0.00007
NM_014989.7(RIMS1):c.1533G>A (p.Pro511=) rs201473375 0.00006
NM_014989.7(RIMS1):c.4506-5G>A rs201556693 0.00006
NM_014989.7(RIMS1):c.1311G>A (p.Arg437=) rs769837216 0.00005
NM_014989.7(RIMS1):c.39C>G (p.Pro13=) rs538562890 0.00003
NM_014989.7(RIMS1):c.4599C>T (p.Thr1533=) rs200818374 0.00003
NM_014989.7(RIMS1):c.458A>C (p.Asn153Thr) rs552482751 0.00001
NM_014989.7(RIMS1):c.4842A>G (p.Pro1614=) rs376289027 0.00001
NM_014989.7(RIMS1):c.1362T>C (p.His454=) rs758749274
NM_014989.7(RIMS1):c.165-3del rs766721792
NM_014989.7(RIMS1):c.1679-12del
NM_014989.7(RIMS1):c.1679-12dup
NM_014989.7(RIMS1):c.1719C>T (p.His573=)
NM_014989.7(RIMS1):c.1958-10dup rs761135970
NM_014989.7(RIMS1):c.2081+15del
NM_014989.7(RIMS1):c.2082-3del
NM_014989.7(RIMS1):c.2242-15C>T
NM_014989.7(RIMS1):c.2372+15del
NM_014989.7(RIMS1):c.2372+18A>G
NM_014989.7(RIMS1):c.2372+27del rs199898147
NM_014989.7(RIMS1):c.2372+27dup rs199898147
NM_014989.7(RIMS1):c.246-6G>A
NM_014989.7(RIMS1):c.3308+84_3308+86del rs200346289
NM_014989.7(RIMS1):c.3465G>C (p.Ala1155=) rs190562383
NM_014989.7(RIMS1):c.435C>A (p.Gly145=) rs566900718
NM_014989.7(RIMS1):c.459+12A>G rs552585116
NM_014989.7(RIMS1):c.4618+19_4618+20del rs113359739
NM_014989.7(RIMS1):c.4618+20del rs113359739
NM_014989.7(RIMS1):c.4618+20dup rs113359739
NM_014989.7(RIMS1):c.4860+80_4860+81del rs67994138

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