ClinVar Miner

List of variants reported as uncertain significance for Cardiac arrhythmia by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_016492.5(RANGRF):c.52C>T (p.Leu18Phe) rs150856064 0.00070
NM_016492.5(RANGRF):c.77+5G>A rs369372561 0.00027
NM_016492.5(RANGRF):c.364G>A (p.Val122Met) rs151189313 0.00014
NM_016492.5(RANGRF):c.434C>T (p.Pro145Leu) rs201882524 0.00006
NM_016492.5(RANGRF):c.428A>G (p.Asn143Ser) rs200615633 0.00005
NM_016492.5(RANGRF):c.535G>A (p.Asp179Asn) rs374174477 0.00004
NM_016492.5(RANGRF):c.132C>A (p.Asp44Glu) rs762109580 0.00003
NM_016492.5(RANGRF):c.249G>C (p.Glu83Asp) rs751751942 0.00003
NM_016492.5(RANGRF):c.437C>T (p.Pro146Leu) rs765772294 0.00003
NM_016492.5(RANGRF):c.50T>A (p.Ile17Asn) rs764464019 0.00003
NM_016492.5(RANGRF):c.342A>T (p.Glu114Asp) rs746452604 0.00002
NM_016492.5(RANGRF):c.128C>T (p.Thr43Met) rs769218673 0.00001
NM_016492.5(RANGRF):c.143T>C (p.Ile48Thr) rs1322326186 0.00001
NM_016492.5(RANGRF):c.250T>G (p.Ser84Ala) rs755244411 0.00001
NM_016492.5(RANGRF):c.256C>T (p.Gln86Ter) rs199622161 0.00001
NM_016492.5(RANGRF):c.293G>A (p.Arg98His) rs778079030 0.00001
NM_016492.5(RANGRF):c.2T>A (p.Met1Lys) rs1230132538 0.00001
NM_016492.5(RANGRF):c.358A>T (p.Lys120Ter) rs1470351437 0.00001
NM_016492.5(RANGRF):c.389G>A (p.Arg130Lys) rs546562640 0.00001
NM_016492.5(RANGRF):c.398A>G (p.Gln133Arg) rs770731506 0.00001
NM_016492.5(RANGRF):c.95C>T (p.Pro32Leu) rs200041073 0.00001
NC_000017.10:g.(?_8192107)_(8192410_?)dup
NC_000017.10:g.(?_8192107)_(8193254_?)dup
NM_016492.5(RANGRF):c.100A>G (p.Asn34Asp)
NM_016492.5(RANGRF):c.109G>A (p.Val37Ile) rs1247874145
NM_016492.5(RANGRF):c.11C>G (p.Thr4Arg) rs1236530787
NM_016492.5(RANGRF):c.134A>G (p.Gln45Arg)
NM_016492.5(RANGRF):c.142del (p.Leu47_Ile48insTer) rs2151608535
NM_016492.5(RANGRF):c.148G>A (p.Glu50Lys) rs1380032341
NM_016492.5(RANGRF):c.155T>C (p.Leu52Pro) rs2151608591
NM_016492.5(RANGRF):c.157_158delinsTT (p.Glu53Leu)
NM_016492.5(RANGRF):c.162_163delinsAT (p.Gln55Ter)
NM_016492.5(RANGRF):c.167C>A (p.Ala56Asp)
NM_016492.5(RANGRF):c.167C>T (p.Ala56Val)
NM_016492.5(RANGRF):c.16_17del (p.Asp6fs) rs752068609
NM_016492.5(RANGRF):c.172G>T (p.Val58Leu)
NM_016492.5(RANGRF):c.173T>A (p.Val58Glu)
NM_016492.5(RANGRF):c.175C>G (p.Arg59Gly)
NM_016492.5(RANGRF):c.175C>T (p.Arg59Trp)
NM_016492.5(RANGRF):c.176G>C (p.Arg59Pro) rs750625803
NM_016492.5(RANGRF):c.176G>T (p.Arg59Leu)
NM_016492.5(RANGRF):c.179G>A (p.Gly60Asp)
NM_016492.5(RANGRF):c.185C>G (p.Ala62Gly) rs1270315228
NM_016492.5(RANGRF):c.190G>A (p.Ala64Thr)
NM_016492.5(RANGRF):c.194+6G>T
NM_016492.5(RANGRF):c.194G>T (p.Arg65Leu) rs1478013092
NM_016492.5(RANGRF):c.197A>G (p.Tyr66Cys)
NM_016492.5(RANGRF):c.198C>A (p.Tyr66Ter)
NM_016492.5(RANGRF):c.202T>A (p.Phe68Ile)
NM_016492.5(RANGRF):c.208G>A (p.Asp70Asn)
NM_016492.5(RANGRF):c.20G>T (p.Cys7Phe)
NM_016492.5(RANGRF):c.238G>A (p.Val80Ile)
NM_016492.5(RANGRF):c.242A>G (p.His81Arg)
NM_016492.5(RANGRF):c.247G>A (p.Glu83Lys)
NM_016492.5(RANGRF):c.301G>A (p.Glu101Lys)
NM_016492.5(RANGRF):c.351+4_351+19del
NM_016492.5(RANGRF):c.351+6G>A
NM_016492.5(RANGRF):c.356C>A (p.Ala119Glu)
NM_016492.5(RANGRF):c.35G>A (p.Gly12Asp) rs1990240045
NM_016492.5(RANGRF):c.371_373del (p.Leu124del) rs989144688
NM_016492.5(RANGRF):c.397C>T (p.Gln133Ter)
NM_016492.5(RANGRF):c.418C>G (p.Leu140Val)
NM_016492.5(RANGRF):c.429T>A (p.Asn143Lys)
NM_016492.5(RANGRF):c.433C>A (p.Pro145Thr)
NM_016492.5(RANGRF):c.437+3A>G rs1597441839
NM_016492.5(RANGRF):c.437+9G>T
NM_016492.5(RANGRF):c.437delC (p.Pro147fs) rs2151610404
NM_016492.5(RANGRF):c.442G>C (p.Asp148His) rs1990342112
NM_016492.5(RANGRF):c.476C>T (p.Ser159Leu)
NM_016492.5(RANGRF):c.484C>T (p.Pro162Ser)
NM_016492.5(RANGRF):c.494T>C (p.Leu165Pro)
NM_016492.5(RANGRF):c.523C>G (p.Leu175Val)
NM_016492.5(RANGRF):c.52C>A (p.Leu18Ile) rs150856064
NM_016492.5(RANGRF):c.534C>G (p.His178Gln)
NM_016492.5(RANGRF):c.535G>T (p.Asp179Tyr) rs374174477
NM_016492.5(RANGRF):c.551G>T (p.Gly184Val) rs547041882
NM_016492.5(RANGRF):c.58A>T (p.Met20Leu) rs1597439817
NM_016492.5(RANGRF):c.59T>C (p.Met20Thr) rs900647124
NM_016492.5(RANGRF):c.5A>G (p.Glu2Gly)
NM_016492.5(RANGRF):c.64dup (p.Ala22fs) rs767541224
NM_016492.5(RANGRF):c.67A>G (p.Ile23Val)
NM_016492.5(RANGRF):c.67A>T (p.Ile23Phe)
NM_016492.5(RANGRF):c.92T>G (p.Val31Gly)
NM_016492.5(RANGRF):c.97G>T (p.Asp33Tyr) rs2151608419

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