ClinVar Miner

List of variants in gene RIMS1 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 125
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HGVS dbSNP
NC_000006.11:g.72889337A>G
NC_000006.11:g.72889412T>G
NC_000006.11:g.72889445A>G
NC_000006.11:g.72889454G>T
NC_000006.11:g.72889472A>T
NC_000006.11:g.72889514C>T
NC_000006.11:g.72889607T>C
NC_000006.11:g.72892050C>G
NC_000006.11:g.72892080G>A
NC_000006.11:g.72892089C>G
NC_000006.11:g.72892191G>C
NC_000006.11:g.72892341C>G
NC_000006.11:g.72892368C>G
NC_000006.11:g.72892401C>T
NC_000006.11:g.72892419G>A
NC_000006.11:g.72892425C>A
NC_000006.11:g.72892437G>T
NC_000006.11:g.72892461G>C
NC_000006.11:g.72892494C>A
NC_000006.11:g.72892623C>T
NC_000006.11:g.72892725C>T
NM_001168407.2(RIMS1):c.101-18T>G
NM_001168407.2(RIMS1):c.101-9A>T
NM_001168407.2(RIMS1):c.1116A>G (p.Leu372=)
NM_001168407.2(RIMS1):c.1120+13C>G
NM_001168407.2(RIMS1):c.1149C>A (p.Ile383=)
NM_001168407.2(RIMS1):c.1161G>A (p.Glu387=)
NM_001168407.2(RIMS1):c.1287T>A (p.Pro429=)
NM_001168407.2(RIMS1):c.1383T>C (p.Arg461=)
NM_001168407.2(RIMS1):c.1401T>C (p.His467=)
NM_001168407.2(RIMS1):c.1535+8C>T
NM_001168407.2(RIMS1):c.1536-464C>T
NM_001168407.2(RIMS1):c.1536-471T>C
NM_001168407.2(RIMS1):c.1536-900C>A
NM_001168407.2(RIMS1):c.1536-963del rs587783021
NM_001168407.2(RIMS1):c.1625+8324T>C
NM_001168407.2(RIMS1):c.1625+8391T>G
NM_001168407.2(RIMS1):c.1698-1057C>T
NM_001168407.2(RIMS1):c.1698-1080C>G
NM_001168407.2(RIMS1):c.1698-1084G>A
NM_001168407.2(RIMS1):c.1737A>G (p.Ala579=)
NM_001168407.2(RIMS1):c.1743A>T (p.Thr581=)
NM_001168407.2(RIMS1):c.1764A>G (p.Gly588=)
NM_001168407.2(RIMS1):c.1767A>G (p.Arg589=)
NM_001168407.2(RIMS1):c.1794C>T (p.Ser598=)
NM_001168407.2(RIMS1):c.1797C>A (p.Gly599=)
NM_001168407.2(RIMS1):c.1811-4G>A
NM_001168407.2(RIMS1):c.2454C>T (p.Ser818=)
NM_001168407.2(RIMS1):c.2465+18G>A
NM_001168407.2(RIMS1):c.2578+10A>T
NM_001168407.2(RIMS1):c.2579-8A>C
NM_001168407.2(RIMS1):c.2680+8G>A
NM_001168407.2(RIMS1):c.2681-10C>T
NM_001168407.2(RIMS1):c.2691C>T (p.Val897=)
NM_001168407.2(RIMS1):c.2781_2782delinsCT (p.Ser927_Leu928=)
NM_001168407.2(RIMS1):c.2787T>G (p.Val929=)
NM_001168407.2(RIMS1):c.2820+10_2820+13del
NM_001168407.2(RIMS1):c.2898C>T (p.Leu966=)
NM_001168407.2(RIMS1):c.2919C>T (p.Ile973=)
NM_001168407.2(RIMS1):c.2928C>T (p.Tyr976=)
NM_001168407.2(RIMS1):c.379+13T>A
NM_001168407.2(RIMS1):c.456A>G (p.Glu152=)
NM_001168407.2(RIMS1):c.504-17T>C
NM_001168407.2(RIMS1):c.636C>T (p.Ala212=)
NM_001168407.2(RIMS1):c.712C>T (p.Leu238=)
NM_001168407.2(RIMS1):c.816C>A (p.Thr272=)
NM_001168407.2(RIMS1):c.990G>A (p.Ala330=)
NM_001168408.2(RIMS1):c.1629-7875G>A
NM_001168408.2(RIMS1):c.1741+15320C>A
NM_001168408.2(RIMS1):c.1741+21540C>T
NM_001168408.2(RIMS1):c.1741+21543C>G
NM_001168408.2(RIMS1):c.1741+21546T>A rs759878173
NM_001168408.2(RIMS1):c.1741+41605C>A
NM_001168408.2(RIMS1):c.1741+41641C>T
NM_001168409.2(RIMS1):c.-109G>A
NM_001168409.2(RIMS1):c.-91A>G
NM_001168411.2(RIMS1):c.-49G>A
NM_001350411.1(RIMS1):c.123C>T (p.Asp41=)
NM_001350411.1(RIMS1):c.13G>C (p.Val5Leu)
NM_001350411.1(RIMS1):c.165-7G>A
NM_001350411.1(RIMS1):c.246-14C>G
NM_001350411.1(RIMS1):c.246-1G>A
NM_001350411.1(RIMS1):c.252T>C (p.His84=)
NM_001350411.1(RIMS1):c.33C>A (p.Arg11=)
NM_001350411.1(RIMS1):c.45G>A (p.Val15=)
NM_001350411.1(RIMS1):c.54C>A (p.Pro18=)
NM_001350411.1(RIMS1):c.87C>T (p.Thr29=)
NM_001350412.1(RIMS1):c.164+81842A>C
NM_014989.5(RIMS1):c.1230C>G (p.Gly410=) rs544554763
NM_014989.5(RIMS1):c.165-8C>T rs569516900
NM_014989.5(RIMS1):c.1678+10C>T rs776366319
NM_014989.5(RIMS1):c.1679-16555A>G rs547118232
NM_014989.5(RIMS1):c.1679-9A>G rs1589870304
NM_014989.5(RIMS1):c.169G>C (p.Val57Leu) rs200005095
NM_014989.5(RIMS1):c.1833C>T (p.Asp611=) rs1589942630
NM_014989.5(RIMS1):c.1890A>C (p.Arg630=) rs1590028055
NM_014989.5(RIMS1):c.1908C>T (p.Thr636=) rs766715883
NM_014989.5(RIMS1):c.1989C>G (p.Pro663=) rs1590192769
NM_014989.5(RIMS1):c.2294A>G (p.Gln765Arg) rs199629596
NM_014989.5(RIMS1):c.2367T>C (p.Asp789=) rs370823273
NM_014989.5(RIMS1):c.2370A>G (p.Arg790=)
NM_014989.5(RIMS1):c.2372+9T>C rs1307382580
NM_014989.5(RIMS1):c.2523A>G (p.Glu841=) rs186078277
NM_014989.5(RIMS1):c.2545-4T>C
NM_014989.5(RIMS1):c.2874C>T (p.Arg958=) rs77297702
NM_014989.5(RIMS1):c.2890A>G (p.Lys964Glu)
NM_014989.5(RIMS1):c.28C>T (p.Pro10Ser) rs200935038
NM_014989.5(RIMS1):c.3069G>A (p.Leu1023=) rs763216349
NM_014989.5(RIMS1):c.3144A>G (p.Leu1048=) rs1157529804
NM_014989.5(RIMS1):c.3465G>A (p.Ala1155=) rs190562383
NM_014989.5(RIMS1):c.3588C>T (p.His1196=) rs762158019
NM_014989.5(RIMS1):c.3758C>T (p.Pro1253Leu)
NM_014989.5(RIMS1):c.3786G>A (p.Ser1262=) rs369147538
NM_014989.5(RIMS1):c.402T>C (p.Tyr134=) rs767877250
NM_014989.5(RIMS1):c.4191G>A (p.Lys1397=) rs372513852
NM_014989.5(RIMS1):c.4197C>T (p.Thr1399=) rs201885523
NM_014989.5(RIMS1):c.423G>A (p.Ala141=)
NM_014989.5(RIMS1):c.4317T>C (p.Val1439=) rs372862808
NM_014989.5(RIMS1):c.4455G>A (p.Pro1485=) rs765647581
NM_014989.5(RIMS1):c.4674T>C (p.Ile1558=) rs1596374235
NM_014989.5(RIMS1):c.561A>G (p.Thr187=) rs746569613
NM_014989.5(RIMS1):c.642G>A (p.Glu214=) rs371815320
NM_014989.5(RIMS1):c.672A>G (p.Thr224=) rs778273984
NM_014989.5(RIMS1):c.798A>G (p.Glu266=) rs755868505
NM_014989.5(RIMS1):c.812+10C>A rs757648777

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