ClinVar Miner

List of variants in gene RIMS1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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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.*1038A>G rs2815736 0.52128
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.*1964C>A rs1055270 0.13021
NM_014989.7(RIMS1):c.*1494T>C rs73750480 0.11554
NM_014989.7(RIMS1):c.*1076A>G rs9446638 0.11417
NM_014989.7(RIMS1):c.3470C>T (p.Pro1157Leu) rs41265501 0.02304
NM_014989.7(RIMS1):c.1776G>A (p.Glu592=) rs77121218 0.01826
NM_014989.7(RIMS1):c.*75G>A rs11751101 0.01731
NM_014989.7(RIMS1):c.743C>T (p.Ser248Leu) rs116476753 0.01524
NM_014989.7(RIMS1):c.*280C>T rs9446637 0.01505
NM_014989.7(RIMS1):c.*138G>T rs55642181 0.00886
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.*2125G>C rs138055062 0.00491
NM_014989.7(RIMS1):c.*2251G>A rs116453051 0.00452
NM_014989.7(RIMS1):c.*1991T>G rs41265503 0.00445
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.3308+12T>G rs115294253 0.00192
NM_014989.7(RIMS1):c.3171C>T (p.Ser1057=) rs201355521 0.00174
NM_014989.7(RIMS1):c.*283A>G rs140634975 0.00168
NM_014989.7(RIMS1):c.*1935A>G rs115062476 0.00159
NM_014989.7(RIMS1):c.594A>G (p.Thr198=) rs149442461 0.00147
NM_014989.7(RIMS1):c.3465G>A (p.Ala1155=) rs190562383 0.00108
NM_014989.7(RIMS1):c.2699-8T>C rs149883454 0.00100
NM_014989.7(RIMS1):c.2367T>C (p.Asp789=) rs370823273 0.00077
NM_014989.7(RIMS1):c.813-14T>G rs180682682 0.00058
NM_014989.7(RIMS1):c.-140T>C rs528494309 0.00049
NM_014989.7(RIMS1):c.3786G>A (p.Ser1262=) rs369147538 0.00046
NM_014989.7(RIMS1):c.*2291C>T rs78214534 0.00032
NM_014989.7(RIMS1):c.942G>A (p.Arg314=) rs185069362 0.00025
NM_014989.7(RIMS1):c.*1458A>T rs549225918 0.00023
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.*1310A>G rs191038983 0.00015
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.28C>T (p.Pro10Ser) rs200935038 0.00005
NM_014989.7(RIMS1):c.*783G>A rs150486970 0.00001
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.*1453dup rs537509888
NM_014989.7(RIMS1):c.*2049T>A rs542135172
NM_014989.7(RIMS1):c.*2429G>A rs570975514
NM_014989.7(RIMS1):c.459+12A>G rs552585116
NM_014989.7(RIMS1):c.4618+20del rs113359739

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