ClinVar Miner

List of variants in gene RINT1 reported as benign by Invitae

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Gene type:
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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_021930.6(RINT1):c.118A>T (p.Ser40Cys) rs11556986 0.19903
NM_021930.6(RINT1):c.414G>A (p.Ala138=) rs7805216 0.05545
NM_021930.6(RINT1):c.840-5G>A rs113947297 0.02749
NM_021930.6(RINT1):c.1374T>C (p.Ala458=) rs35961194 0.01433
NM_021930.6(RINT1):c.1471+10T>C rs117732387 0.00885
NM_021930.6(RINT1):c.732C>T (p.Ile244=) rs148050825 0.00603
NM_021930.6(RINT1):c.465C>T (p.Ile155=) rs79893877 0.00578
NM_021930.6(RINT1):c.375T>C (p.Thr125=) rs34064404 0.00507
NM_021930.6(RINT1):c.783G>A (p.Pro261=) rs144905970 0.00048
NM_021930.6(RINT1):c.1025T>C (p.Met342Thr) rs140651827 0.00031
NM_021930.6(RINT1):c.1101C>T (p.Asn367=) rs770071693 0.00004
NM_021930.6(RINT1):c.1656T>C (p.Asp552=) rs192297021 0.00004
NM_021930.6(RINT1):c.543C>T (p.Thr181=) rs774063327 0.00004
NM_021930.6(RINT1):c.274-15del rs151160374
NM_021930.6(RINT1):c.43-12TTC[2] rs374498388
NM_021930.6(RINT1):c.89-8del
NM_021930.6(RINT1):c.997-14del rs2133399882

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