ClinVar Miner

List of variants in gene RIMS1 reported as uncertain significance by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 185
Download table as spreadsheet
HGVS dbSNP
NC_000006.11:g.(?_72974678)_(72975206_?)del
NC_000006.11:g.(?_73016941)_(73023395_?)dup
NC_000006.11:g.72889455C>T
NC_000006.11:g.72889480C>T
NC_000006.11:g.72889527A>G
NC_000006.11:g.72889563G>C
NC_000006.11:g.72892069C>G
NC_000006.11:g.72892079A>C
NC_000006.11:g.72892091A>C
NC_000006.11:g.72892133A>G
NC_000006.11:g.72892270G>A
NC_000006.11:g.72892280C>T
NC_000006.11:g.72892305G>A
NC_000006.11:g.72892353_72892379del
NC_000006.11:g.72892363C>T
NC_000006.11:g.72892415C>G
NC_000006.11:g.72892424C>T
NC_000006.11:g.72892435C>T
NC_000006.11:g.72892502_72892503delinsCC
NC_000006.11:g.72892534C>T
NC_000006.11:g.72892560_72892574del
NC_000006.11:g.72892627C>G
NM_001168407.2(RIMS1):c.1006C>A (p.Pro336Thr)
NM_001168407.2(RIMS1):c.1193-4G>A
NM_001168407.2(RIMS1):c.1220A>G (p.Lys407Arg)
NM_001168407.2(RIMS1):c.1262A>G (p.His421Arg)
NM_001168407.2(RIMS1):c.1396C>G (p.His466Asp)
NM_001168407.2(RIMS1):c.1467A>C (p.Gln489His)
NM_001168407.2(RIMS1):c.1536-484T>G
NM_001168407.2(RIMS1):c.1536-508A>C
NM_001168407.2(RIMS1):c.1536-544C>T
NM_001168407.2(RIMS1):c.1536-562T>G
NM_001168407.2(RIMS1):c.1536-915A>T
NM_001168407.2(RIMS1):c.1536-926C>G
NM_001168407.2(RIMS1):c.1536-954C>A
NM_001168407.2(RIMS1):c.1536-959T>G
NM_001168407.2(RIMS1):c.1536-972C>T
NM_001168407.2(RIMS1):c.1625+8302G>A
NM_001168407.2(RIMS1):c.1625+8302G>C
NM_001168407.2(RIMS1):c.1625+8332G>A
NM_001168407.2(RIMS1):c.1625+8355A>C
NM_001168407.2(RIMS1):c.1625+8389A>G
NM_001168407.2(RIMS1):c.1697+4G>A
NM_001168407.2(RIMS1):c.1698-1085C>T
NM_001168407.2(RIMS1):c.1698-1097C>T
NM_001168407.2(RIMS1):c.1698-1099G>A
NM_001168407.2(RIMS1):c.1698-1100C>T
NM_001168407.2(RIMS1):c.1698-1116C>A
NM_001168407.2(RIMS1):c.1698-1119C>T
NM_001168407.2(RIMS1):c.1698-1227G>A
NM_001168407.2(RIMS1):c.1698-1245A>G
NM_001168407.2(RIMS1):c.1715G>A (p.Ser572Asn)
NM_001168407.2(RIMS1):c.1757G>A (p.Arg586His)
NM_001168407.2(RIMS1):c.1785A>G (p.Pro595=)
NM_001168407.2(RIMS1):c.2420G>A (p.Arg807Gln)
NM_001168407.2(RIMS1):c.245T>C (p.Met82Thr)
NM_001168407.2(RIMS1):c.2820+3C>T
NM_001168407.2(RIMS1):c.2971C>A (p.Pro991Thr)
NM_001168407.2(RIMS1):c.2980C>A (p.Arg994=)
NM_001168407.2(RIMS1):c.2984G>A (p.Arg995Gln)
NM_001168407.2(RIMS1):c.311G>A (p.Arg104Gln)
NM_001168407.2(RIMS1):c.313C>G (p.Leu105Val)
NM_001168407.2(RIMS1):c.748C>T (p.Arg250Cys)
NM_001168407.2(RIMS1):c.827A>G (p.Lys276Arg)
NM_001168408.2(RIMS1):c.1741+15256G>T
NM_001168408.2(RIMS1):c.1741+15284C>A
NM_001168408.2(RIMS1):c.1741+15307C>T
NM_001168408.2(RIMS1):c.1741+15314A>G
NM_001168408.2(RIMS1):c.1741+21499G>A
NM_001168408.2(RIMS1):c.1741+21545T>C
NM_001168408.2(RIMS1):c.1741+21568C>T
NM_001168408.2(RIMS1):c.1741+41607T>C
NM_001168408.2(RIMS1):c.1741+41645C>G
NM_001168408.2(RIMS1):c.1741+41690G>A
NM_001168408.2(RIMS1):c.1741+41729G>A
NM_001168408.2(RIMS1):c.1741+41754G>A
NM_001168409.2(RIMS1):c.-118T>G
NM_001168409.2(RIMS1):c.-44G>A
NM_001168409.2(RIMS1):c.-44G>C
NM_001168409.2(RIMS1):c.-57C>A
NM_001168409.2(RIMS1):c.-65C>T
NM_001168409.2(RIMS1):c.-74A>G
NM_001168409.2(RIMS1):c.-76G>A
NM_001168409.2(RIMS1):c.-98G>A
NM_001168409.2(RIMS1):c.-99C>T
NM_001350411.1(RIMS1):c.13G>T (p.Val5Leu)
NM_001350411.1(RIMS1):c.305G>A (p.Arg102Gln)
NM_001350411.1(RIMS1):c.419C>T (p.Ala140Val)
NM_001350411.1(RIMS1):c.460G>A (p.Asp154Asn)
NM_001350411.1(RIMS1):c.52C>A (p.Pro18Thr)
NM_001350412.1(RIMS1):c.164+81816C>T
NM_001350412.1(RIMS1):c.164+81858A>T
NM_001350412.1(RIMS1):c.164+81869C>T
NM_001350419.2(RIMS1):c.1472+1644T>C
NM_001350419.2(RIMS1):c.1472+1647A>G
NM_001350419.2(RIMS1):c.1472+1652A>G
NM_014989.5(RIMS1):c.1009G>A (p.Gly337Ser)
NM_014989.5(RIMS1):c.1046A>C (p.Glu349Ala)
NM_014989.5(RIMS1):c.104T>C (p.Ile35Thr)
NM_014989.5(RIMS1):c.1088G>T (p.Arg363Leu)
NM_014989.5(RIMS1):c.1151C>T (p.Ala384Val)
NM_014989.5(RIMS1):c.1174G>A (p.Asp392Asn)
NM_014989.5(RIMS1):c.1214C>G (p.Pro405Arg)
NM_014989.5(RIMS1):c.1228G>A (p.Gly410Ser)
NM_014989.5(RIMS1):c.1265_1276dup (p.Pro422_Pro425dup)
NM_014989.5(RIMS1):c.1297A>G (p.Thr433Ala)
NM_014989.5(RIMS1):c.1315C>G (p.Pro439Ala)
NM_014989.5(RIMS1):c.1366C>G (p.Pro456Ala)
NM_014989.5(RIMS1):c.1382C>T (p.Ala461Val) rs886061706
NM_014989.5(RIMS1):c.1405C>G (p.Pro469Ala)
NM_014989.5(RIMS1):c.1534T>C (p.Ser512Pro)
NM_014989.5(RIMS1):c.1567G>T (p.Gly523Cys)
NM_014989.5(RIMS1):c.1630A>G (p.Thr544Ala)
NM_014989.5(RIMS1):c.1744T>G (p.Ser582Ala)
NM_014989.5(RIMS1):c.1892T>C (p.Leu631Pro)
NM_014989.5(RIMS1):c.1956A>G (p.Ala652=)
NM_014989.5(RIMS1):c.1987C>A (p.Pro663Thr)
NM_014989.5(RIMS1):c.2093G>A (p.Arg698Gln)
NM_014989.5(RIMS1):c.2241T>C (p.Ser747=) rs760492397
NM_014989.5(RIMS1):c.2261A>G (p.Lys754Arg)
NM_014989.5(RIMS1):c.2308C>T (p.Pro770Ser)
NM_014989.5(RIMS1):c.2311G>A (p.Ala771Thr)
NM_014989.5(RIMS1):c.2446T>G (p.Ser816Ala)
NM_014989.5(RIMS1):c.2545-3C>T
NM_014989.5(RIMS1):c.2617T>C (p.Ser873Pro)
NM_014989.5(RIMS1):c.2624T>C (p.Leu875Pro)
NM_014989.5(RIMS1):c.2633C>T (p.Pro878Leu)
NM_014989.5(RIMS1):c.2764C>A (p.Pro922Thr)
NM_014989.5(RIMS1):c.2803T>C (p.Ser935Pro)
NM_014989.5(RIMS1):c.2894C>T (p.Pro965Leu) rs752875047
NM_014989.5(RIMS1):c.2963G>A (p.Arg988His)
NM_014989.5(RIMS1):c.2977C>T (p.His993Tyr)
NM_014989.5(RIMS1):c.3016A>G (p.Arg1006Gly)
NM_014989.5(RIMS1):c.3430C>T (p.Arg1144Ter)
NM_014989.5(RIMS1):c.3554+2T>C
NM_014989.5(RIMS1):c.3589G>A (p.Ala1197Thr)
NM_014989.5(RIMS1):c.3703G>A (p.Gly1235Arg)
NM_014989.5(RIMS1):c.3741G>T (p.Met1247Ile)
NM_014989.5(RIMS1):c.376G>T (p.Asp126Tyr)
NM_014989.5(RIMS1):c.3832A>G (p.Ser1278Gly)
NM_014989.5(RIMS1):c.3835G>A (p.Gly1279Ser)
NM_014989.5(RIMS1):c.3850+6C>T
NM_014989.5(RIMS1):c.3921G>T (p.Gly1307=) rs769179703
NM_014989.5(RIMS1):c.4111C>T (p.Arg1371Cys)
NM_014989.5(RIMS1):c.4159C>T (p.Arg1387Trp) rs201017334
NM_014989.5(RIMS1):c.4186A>G (p.Met1396Val)
NM_014989.5(RIMS1):c.436C>T (p.Arg146Cys)
NM_014989.5(RIMS1):c.443C>T (p.Ser148Phe)
NM_014989.5(RIMS1):c.4512A>G (p.Ile1504Met) rs746893761
NM_014989.5(RIMS1):c.459C>T (p.Asn153=)
NM_014989.5(RIMS1):c.460G>C (p.Glu154Gln)
NM_014989.5(RIMS1):c.4668A>C (p.Glu1556Asp)
NM_014989.5(RIMS1):c.4712C>T (p.Ser1571Phe)
NM_014989.5(RIMS1):c.4725A>G (p.Pro1575=)
NM_014989.5(RIMS1):c.4746G>A (p.Leu1582=)
NM_014989.5(RIMS1):c.4835A>C (p.Glu1612Ala)
NM_014989.5(RIMS1):c.4945T>A (p.Ser1649Thr)
NM_014989.5(RIMS1):c.5053A>G (p.Thr1685Ala)
NM_014989.5(RIMS1):c.617G>A (p.Arg206Lys)
NM_014989.5(RIMS1):c.642G>C (p.Glu214Asp)
NM_014989.5(RIMS1):c.647C>T (p.Ser216Leu)
NM_014989.5(RIMS1):c.708C>A (p.Ser236Arg)
NM_014989.5(RIMS1):c.70G>A (p.Asp24Asn)
NM_014989.5(RIMS1):c.72C>G (p.Asp24Glu)
NM_014989.5(RIMS1):c.826G>A (p.Gly276Arg)
NM_014989.5(RIMS1):c.928C>T (p.Arg310Cys)
NM_014989.6(RIMS1):c.1124T>C (p.Met375Thr)
NM_014989.6(RIMS1):c.1309A>G (p.Arg437Gly)
NM_014989.6(RIMS1):c.1450A>G (p.Met484Val)
NM_014989.6(RIMS1):c.1807A>C (p.Asn603His)
NM_014989.6(RIMS1):c.2074C>T (p.Pro692Ser)
NM_014989.6(RIMS1):c.2269C>T (p.His757Tyr)
NM_014989.6(RIMS1):c.2452G>A (p.Val818Ile)
NM_014989.6(RIMS1):c.256C>G (p.Gln86Glu)
NM_014989.6(RIMS1):c.2680T>G (p.Ser894Ala)
NM_014989.6(RIMS1):c.2993G>A (p.Arg998Gln)
NM_014989.6(RIMS1):c.3980A>G (p.Asp1327Gly)
NM_014989.6(RIMS1):c.4112G>A (p.Arg1371His)
NM_014989.6(RIMS1):c.4205G>C (p.Ser1402Thr)
NM_014989.6(RIMS1):c.4391G>C (p.Ser1464Thr)
NM_014989.6(RIMS1):c.4613C>A (p.Ala1538Glu)
NM_014989.6(RIMS1):c.4846G>T (p.Gly1616Cys)
NM_014989.6(RIMS1):c.583G>A (p.Asp195Asn)
NM_014989.6(RIMS1):c.616A>G (p.Arg206Gly)
NM_014989.6(RIMS1):c.986A>G (p.Asp329Gly)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.