ClinVar Miner

List of variants in gene RIN1 studied for not specified

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Gene type:
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Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_004292.3(RIN1):c.1609G>A (p.Asp537Asn) rs145559573 0.00036
NM_004292.3(RIN1):c.893C>G (p.Pro298Arg) rs143733163 0.00031
NM_004292.3(RIN1):c.712C>T (p.Arg238Trp) rs137954374 0.00030
NM_004292.3(RIN1):c.1511G>A (p.Arg504His) rs533409856 0.00026
NM_004292.3(RIN1):c.1271C>T (p.Ser424Leu) rs144912431 0.00023
NM_004292.3(RIN1):c.1772G>A (p.Gly591Asp) rs375956582 0.00017
NM_004292.3(RIN1):c.2245C>T (p.Arg749Trp) rs62619978 0.00016
NM_004292.3(RIN1):c.353C>G (p.Ser118Cys) rs200680197 0.00012
NM_004292.3(RIN1):c.1778G>A (p.Gly593Asp) rs530888270 0.00011
NM_004292.3(RIN1):c.2047C>T (p.Arg683Cys) rs371743923 0.00011
NM_004292.3(RIN1):c.1207C>T (p.Arg403Cys) rs770760023 0.00010
NM_004292.3(RIN1):c.2107C>T (p.Arg703Trp) rs139103405 0.00010
NM_004292.3(RIN1):c.1103C>T (p.Ala368Val) rs754638838 0.00007
NM_004292.3(RIN1):c.130G>A (p.Gly44Arg) rs570029800 0.00007
NM_004292.3(RIN1):c.1396G>A (p.Ala466Thr) rs780519847 0.00007
NM_004292.3(RIN1):c.1823G>A (p.Arg608His) rs573426435 0.00007
NM_004292.3(RIN1):c.50C>T (p.Pro17Leu) rs751627916 0.00007
NM_004292.3(RIN1):c.743G>A (p.Arg248His) rs138640780 0.00005
NM_004292.3(RIN1):c.92C>T (p.Ala31Val) rs777945851 0.00005
NM_004292.3(RIN1):c.1454G>T (p.Ser485Ile) rs749622372 0.00004
NM_004292.3(RIN1):c.576G>T (p.Lys192Asn) rs202131583 0.00004
NM_004292.3(RIN1):c.139G>C (p.Gly47Arg) rs1302420018 0.00003
NM_004292.3(RIN1):c.1408C>T (p.Arg470Cys) rs551098881 0.00003
NM_004292.3(RIN1):c.181C>T (p.Arg61Cys) rs527854146 0.00003
NM_004292.3(RIN1):c.2273G>T (p.Gly758Val) rs765691604 0.00003
NM_004292.3(RIN1):c.580C>G (p.Gln194Glu) rs369402774 0.00003
NM_004292.3(RIN1):c.862C>T (p.Arg288Trp) rs374557872 0.00003
NM_004292.3(RIN1):c.901A>T (p.Ser301Cys) rs199676860 0.00003
NM_004292.3(RIN1):c.1357C>T (p.Arg453Trp) rs750140506 0.00002
NM_004292.3(RIN1):c.1504C>G (p.Leu502Val) rs777535128 0.00002
NM_004292.3(RIN1):c.1850G>A (p.Arg617His) rs775302008 0.00002
NM_004292.3(RIN1):c.583C>T (p.Arg195Trp) rs549656126 0.00002
NM_004292.3(RIN1):c.727A>G (p.Arg243Gly) rs375942445 0.00002
NM_004292.3(RIN1):c.1219A>G (p.Ser407Gly) rs1387319578 0.00001
NM_004292.3(RIN1):c.1222C>T (p.Arg408Trp) rs374038558 0.00001
NM_004292.3(RIN1):c.134A>G (p.Gln45Arg) rs1362524398 0.00001
NM_004292.3(RIN1):c.1486C>T (p.Arg496Cys) rs780527054 0.00001
NM_004292.3(RIN1):c.1568A>G (p.Tyr523Cys) rs770386874 0.00001
NM_004292.3(RIN1):c.1583C>T (p.Thr528Ile) rs1442953912 0.00001
NM_004292.3(RIN1):c.1603G>A (p.Gly535Ser) rs375786858 0.00001
NM_004292.3(RIN1):c.1865A>G (p.His622Arg) rs764870832 0.00001
NM_004292.3(RIN1):c.1913G>C (p.Gly638Ala) rs776967514 0.00001
NM_004292.3(RIN1):c.2029A>G (p.Lys677Glu) rs1854764392 0.00001
NM_004292.3(RIN1):c.2051T>C (p.Leu684Pro) rs370072639 0.00001
NM_004292.3(RIN1):c.2057C>T (p.Pro686Leu) rs1854762931 0.00001
NM_004292.3(RIN1):c.317T>C (p.Met106Thr) rs1308530396 0.00001
NM_004292.3(RIN1):c.319C>T (p.Arg107Trp) rs747513842 0.00001
NM_004292.3(RIN1):c.398G>T (p.Gly133Val) rs140899774 0.00001
NM_004292.3(RIN1):c.442T>C (p.Tyr148His) rs1007821968 0.00001
NM_004292.3(RIN1):c.845C>A (p.Pro282His) rs752344031 0.00001
NM_004292.3(RIN1):c.1015C>A (p.His339Asn)
NM_004292.3(RIN1):c.1025G>A (p.Arg342His)
NM_004292.3(RIN1):c.1037T>C (p.Leu346Pro) rs1854834074
NM_004292.3(RIN1):c.1130C>T (p.Thr377Ile) rs1440156888
NM_004292.3(RIN1):c.1136C>T (p.Ala379Val)
NM_004292.3(RIN1):c.1142A>C (p.Gln381Pro)
NM_004292.3(RIN1):c.1148T>C (p.Val383Ala)
NM_004292.3(RIN1):c.1183G>A (p.Glu395Lys)
NM_004292.3(RIN1):c.1208G>T (p.Arg403Leu) rs201132980
NM_004292.3(RIN1):c.1223G>A (p.Arg408Gln)
NM_004292.3(RIN1):c.1346C>G (p.Ala449Gly) rs1412723743
NM_004292.3(RIN1):c.1358G>A (p.Arg453Gln)
NM_004292.3(RIN1):c.1361G>A (p.Arg454His)
NM_004292.3(RIN1):c.1384C>G (p.Leu462Val)
NM_004292.3(RIN1):c.1394T>C (p.Leu465Pro) rs2495321836
NM_004292.3(RIN1):c.1440C>A (p.Phe480Leu)
NM_004292.3(RIN1):c.1487G>A (p.Arg496His) rs141038581
NM_004292.3(RIN1):c.1487G>T (p.Arg496Leu) rs141038581
NM_004292.3(RIN1):c.1540C>T (p.Arg514Trp)
NM_004292.3(RIN1):c.1581G>C (p.Arg527Ser)
NM_004292.3(RIN1):c.1630A>G (p.Ser544Gly)
NM_004292.3(RIN1):c.2062G>T (p.Ala688Ser)
NM_004292.3(RIN1):c.2105G>A (p.Arg702His)
NM_004292.3(RIN1):c.2162A>T (p.Gln721Leu) rs2495311827
NM_004292.3(RIN1):c.2248G>C (p.Glu750Gln)
NM_004292.3(RIN1):c.2336G>A (p.Arg779Gln)
NM_004292.3(RIN1):c.2338G>A (p.Ala780Thr) rs751629204
NM_004292.3(RIN1):c.247C>A (p.Leu83Met)
NM_004292.3(RIN1):c.256G>A (p.Glu86Lys)
NM_004292.3(RIN1):c.295C>T (p.Arg99Cys) rs576392806
NM_004292.3(RIN1):c.296G>A (p.Arg99His)
NM_004292.3(RIN1):c.320G>A (p.Arg107Gln)
NM_004292.3(RIN1):c.331G>A (p.Ala111Thr)
NM_004292.3(RIN1):c.336T>G (p.Ser112Arg) rs567439359
NM_004292.3(RIN1):c.401C>T (p.Ser134Leu)
NM_004292.3(RIN1):c.457G>A (p.Asp153Asn)
NM_004292.3(RIN1):c.502G>A (p.Ala168Thr)
NM_004292.3(RIN1):c.512A>G (p.His171Arg)
NM_004292.3(RIN1):c.604G>A (p.Val202Met) rs1249146965
NM_004292.3(RIN1):c.661G>T (p.Ala221Ser) rs768448722
NM_004292.3(RIN1):c.689C>G (p.Pro230Arg) rs545135172
NM_004292.3(RIN1):c.745G>A (p.Val249Met)
NM_004292.3(RIN1):c.770T>C (p.Leu257Pro)
NM_004292.3(RIN1):c.828C>G (p.Ser276Arg)
NM_004292.3(RIN1):c.82G>C (p.Glu28Gln)
NM_004292.3(RIN1):c.863G>A (p.Arg288Gln)
NM_004292.3(RIN1):c.868G>A (p.Glu290Lys) rs1207023402
NM_004292.3(RIN1):c.877G>A (p.Val293Met)
NM_004292.3(RIN1):c.886C>T (p.Arg296Cys)
NM_004292.3(RIN1):c.889G>T (p.Val297Leu)
NM_004292.3(RIN1):c.898G>T (p.Gly300Cys) rs377286544
NM_004292.3(RIN1):c.910A>C (p.Ser304Arg) rs2495328188
NM_004292.3(RIN1):c.917C>T (p.Pro306Leu)
NM_004292.3(RIN1):c.967G>A (p.Glu323Lys) rs779648226
NM_004292.3(RIN1):c.979G>A (p.Val327Met)

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