ClinVar Miner

List of variants in gene MOCS2 reported as uncertain significance for not provided

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Gene type:
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Total variants: 93
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HGVS dbSNP gnomAD frequency
NM_004531.5(MOCS2):c.367C>T (p.His123Tyr) rs2233218 0.00399
NM_004531.5(MOCS2):c.108G>A (p.Met36Ile) rs140563222 0.00064
NM_004531.5(MOCS2):c.296C>T (p.Ala99Val) rs2233217 0.00049
NM_176806.4(MOCS2):c.178C>T (p.Arg60Cys) rs146074751 0.00045
NM_004531.5(MOCS2):c.*837T>C rs546218674 0.00021
NM_004531.5(MOCS2):c.209C>T (p.Ala70Val) rs148685617 0.00015
NM_176806.4(MOCS2):c.56C>G (p.Thr19Arg) rs372782831 0.00014
NM_176806.4(MOCS2):c.146C>G (p.Ala49Gly) rs766341488 0.00011
NM_004531.5(MOCS2):c.163T>G (p.Ser55Ala) rs1375036528 0.00008
NM_004531.5(MOCS2):c.154G>A (p.Glu52Lys) rs769972877 0.00006
NM_004531.5(MOCS2):c.464T>C (p.Ile155Thr) rs143347340 0.00006
NM_004531.5(MOCS2):c.499A>C (p.Lys167Gln) rs776534922 0.00006
NM_176806.4(MOCS2):c.45T>A (p.Ser15Arg) rs1554028127 0.00005
NM_004531.5(MOCS2):c.107T>C (p.Met36Thr) rs774862394 0.00004
NM_004531.5(MOCS2):c.226G>A (p.Gly76Arg) rs780085174 0.00004
NM_004531.5(MOCS2):c.241A>T (p.Asn81Tyr) rs555716628 0.00004
NM_004531.5(MOCS2):c.415G>A (p.Val139Met) rs199581021 0.00004
NM_004531.5(MOCS2):c.325G>A (p.Asp109Asn) rs774737022 0.00003
NM_004531.5(MOCS2):c.523A>G (p.Thr175Ala) rs1394110943 0.00003
NM_004531.5(MOCS2):c.550T>G (p.Trp184Gly) rs747390142 0.00003
NM_004531.5(MOCS2):c.197C>T (p.Pro66Leu) rs371082200 0.00002
NM_004531.5(MOCS2):c.59C>T (p.Ser20Phe) rs983241087 0.00002
NM_004531.5(MOCS2):c.74A>G (p.Glu25Gly) rs749876758 0.00002
NM_004531.5(MOCS2):c.121G>A (p.Glu41Lys) rs766056977 0.00001
NM_004531.5(MOCS2):c.128C>A (p.Ser43Tyr) rs371126072 0.00001
NM_004531.5(MOCS2):c.140T>C (p.Ile47Thr) rs146784991 0.00001
NM_004531.5(MOCS2):c.233C>T (p.Thr78Ile) rs989688918 0.00001
NM_004531.5(MOCS2):c.284A>T (p.Tyr95Phe) rs754241121 0.00001
NM_004531.5(MOCS2):c.419C>T (p.Ser140Phe) rs914249018 0.00001
NM_004531.5(MOCS2):c.433G>C (p.Ala145Pro) rs150503623 0.00001
NM_004531.5(MOCS2):c.472_477del (p.Leu158_Lys159del) rs770831815 0.00001
NM_004531.5(MOCS2):c.511G>A (p.Glu171Lys) rs766166640 0.00001
NM_004531.5(MOCS2):c.539A>G (p.Lys180Arg) rs200534063 0.00001
NM_004531.5(MOCS2):c.57A>T (p.Leu19Phe) rs776441627 0.00001
NM_004531.5(MOCS2):c.61C>T (p.Pro21Ser) rs1379732256 0.00001
NM_176806.4(MOCS2):c.163A>G (p.Ile55Val) rs1240805422 0.00001
NM_176806.4(MOCS2):c.179G>A (p.Arg60His) rs769172548 0.00001
NM_176806.4(MOCS2):c.61G>T (p.Val21Phe) rs759021832 0.00001
NM_004531.5(MOCS2):c.118G>A (p.Glu40Lys)
NM_004531.5(MOCS2):c.136G>A (p.Val46Ile)
NM_004531.5(MOCS2):c.149C>G (p.Thr50Ser)
NM_004531.5(MOCS2):c.160C>G (p.Leu54Val)
NM_004531.5(MOCS2):c.169G>T (p.Asp57Tyr)
NM_004531.5(MOCS2):c.206G>A (p.Gly69Asp) rs754818995
NM_004531.5(MOCS2):c.239A>G (p.Asn80Ser)
NM_004531.5(MOCS2):c.244T>G (p.Phe82Val) rs1579932680
NM_004531.5(MOCS2):c.294G>T (p.Met98Ile)
NM_004531.5(MOCS2):c.302A>G (p.Asn101Ser)
NM_004531.5(MOCS2):c.319T>G (p.Cys107Gly) rs2112083286
NM_004531.5(MOCS2):c.322A>G (p.Ser108Gly)
NM_004531.5(MOCS2):c.33C>A (p.Phe11Leu)
NM_004531.5(MOCS2):c.344C>T (p.Pro115Leu)
NM_004531.5(MOCS2):c.377+5G>C
NM_004531.5(MOCS2):c.377G>C (p.Gly126Ala) rs1433384442
NM_004531.5(MOCS2):c.389T>G (p.Val130Gly)
NM_004531.5(MOCS2):c.402C>G (p.Ser134Arg)
NM_004531.5(MOCS2):c.411T>G (p.Ile137Met)
NM_004531.5(MOCS2):c.428A>G (p.His143Arg)
NM_004531.5(MOCS2):c.460G>A (p.Ala154Thr)
NM_004531.5(MOCS2):c.473T>G (p.Leu158Ter)
NM_004531.5(MOCS2):c.479C>T (p.Ala160Val) rs1740875690
NM_004531.5(MOCS2):c.487C>T (p.Pro163Ser) rs534504858
NM_004531.5(MOCS2):c.4T>G (p.Ser2Ala)
NM_004531.5(MOCS2):c.500del (p.Lys167fs) rs2112081965
NM_004531.5(MOCS2):c.501+4A>G rs1740874146
NM_004531.5(MOCS2):c.501G>A (p.Lys167=)
NM_004531.5(MOCS2):c.507A>G (p.Ile169Met)
NM_004531.5(MOCS2):c.509A>G (p.Tyr170Cys) rs755284842
NM_004531.5(MOCS2):c.512A>G (p.Glu171Gly)
NM_004531.5(MOCS2):c.514G>C (p.Glu172Gln) rs1246273723
NM_004531.5(MOCS2):c.550T>C (p.Trp184Arg)
NM_004531.5(MOCS2):c.63C>G (p.Pro21=)
NM_004531.5(MOCS2):c.64C>G (p.Pro22Ala) rs995972455
NM_004531.5(MOCS2):c.6G>A (p.Ser2=) rs1300378829
NM_004531.5(MOCS2):c.77A>T (p.Asp26Val)
NM_004531.5(MOCS2):c.78T>C (p.Asp26=)
NM_004531.5(MOCS2):c.81T>G (p.Ser27Arg)
NM_004531.5(MOCS2):c.82G>A (p.Ala28Thr)
NM_004531.5(MOCS2):c.85T>C (p.Phe29Leu)
NM_176806.4(MOCS2):c.100G>T (p.Ala34Ser) rs2112092902
NM_176806.4(MOCS2):c.109C>G (p.Leu37Val) rs2112092880
NM_176806.4(MOCS2):c.117G>T (p.Lys39Asn)
NM_176806.4(MOCS2):c.126A>C (p.Glu42Asp)
NM_176806.4(MOCS2):c.161A>G (p.Gln54Arg) rs774169356
NM_176806.4(MOCS2):c.170T>C (p.Phe57Ser)
NM_176806.4(MOCS2):c.183A>G (p.Gln61=) rs2112090960
NM_176806.4(MOCS2):c.30G>T (p.Leu10Phe)
NM_176806.4(MOCS2):c.38C>G (p.Ala13Gly) rs778448083
NM_176806.4(MOCS2):c.42A>T (p.Lys14Asn)
NM_176806.4(MOCS2):c.65G>C (p.Arg22Pro) rs577168655
NM_176806.4(MOCS2):c.65G>T (p.Arg22Leu) rs577168655
NM_176806.4(MOCS2):c.76A>G (p.Ile26Val)
NM_176806.4(MOCS2):c.79T>C (p.Ser27Pro) rs1579937471

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