ClinVar Miner

List of variants in gene ACADM reported as uncertain significance by Invitae

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Gene type:
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Total variants: 106
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HGVS dbSNP gnomAD frequency
NM_000016.6(ACADM):c.127G>A (p.Glu43Lys) rs147559466 0.00210
NM_000016.6(ACADM):c.1091T>C (p.Ile364Thr) rs150710061 0.00031
NM_000016.6(ACADM):c.214G>A (p.Glu72Lys) rs374358376 0.00028
NM_000016.6(ACADM):c.508G>T (p.Ala170Ser) rs763613689 0.00013
NM_000016.6(ACADM):c.1022C>G (p.Ala341Gly) rs768440594 0.00006
NM_000016.6(ACADM):c.1265A>T (p.Ter422Leu) rs200376609 0.00006
NM_000016.6(ACADM):c.131A>G (p.Gln44Arg) rs751647383 0.00006
NM_000016.6(ACADM):c.50G>A (p.Arg17His) rs17848070 0.00004
NM_000016.6(ACADM):c.286G>C (p.Gly96Arg) rs886042055 0.00003
NM_000016.6(ACADM):c.1125A>G (p.Ile375Met) rs201809827 0.00002
NM_000016.6(ACADM):c.393G>A (p.Met131Ile) rs368773005 0.00002
NM_000016.6(ACADM):c.1090A>G (p.Ile364Val) rs758973773 0.00001
NM_000016.6(ACADM):c.1194+3A>G rs369945009 0.00001
NM_000016.6(ACADM):c.1216A>G (p.Ile406Val) rs1181589709 0.00001
NM_000016.6(ACADM):c.1257C>A (p.Tyr419Ter) rs753928772 0.00001
NM_000016.6(ACADM):c.125C>T (p.Thr42Ile) rs759997176 0.00001
NM_000016.6(ACADM):c.206A>T (p.Lys69Ile) rs927784210 0.00001
NM_000016.6(ACADM):c.271_273del (p.Ile91del) rs1463718964 0.00001
NM_000016.6(ACADM):c.277G>A (p.Glu93Lys) rs752612962 0.00001
NM_000016.6(ACADM):c.296G>T (p.Gly99Val) rs370608001 0.00001
NM_000016.6(ACADM):c.554T>G (p.Ile185Ser) rs1647480996 0.00001
NM_000016.6(ACADM):c.56A>G (p.His19Arg) rs1446893994 0.00001
NM_000016.6(ACADM):c.581A>G (p.Asn194Ser) rs1010454733 0.00001
NM_000016.6(ACADM):c.661G>A (p.Gly221Arg) rs753627680 0.00001
NM_000016.6(ACADM):c.667A>G (p.Ile223Val) rs747783631 0.00001
NC_000001.10:g.(?_76190473)_(76228448_?)dup
NC_000001.10:g.(?_76205645)_(76228448_?)dup
NM_000016.6(ACADM):c.*5delA
NM_000016.6(ACADM):c.1007G>A (p.Ser336Asn) rs794727013
NM_000016.6(ACADM):c.1012C>G (p.Gln338Glu) rs796051896
NM_000016.6(ACADM):c.101G>T (p.Gly34Val)
NM_000016.6(ACADM):c.1021G>A (p.Ala341Thr) rs1424545377
NM_000016.6(ACADM):c.1043G>A (p.Arg348His)
NM_000016.6(ACADM):c.1070C>G (p.Ala357Gly)
NM_000016.6(ACADM):c.1075G>C (p.Ala359Pro) rs1224909875
NM_000016.6(ACADM):c.10G>A (p.Gly4Arg)
NM_000016.6(ACADM):c.1117G>C (p.Val373Leu)
NM_000016.6(ACADM):c.1159G>C (p.Val387Leu) rs1057518630
NM_000016.6(ACADM):c.1184A>C (p.Lys395Thr) rs776312173
NM_000016.6(ACADM):c.119-12A>G
NM_000016.6(ACADM):c.1194+6G>A
NM_000016.6(ACADM):c.1197T>G (p.Ile399Met)
NM_000016.6(ACADM):c.11G>T (p.Gly4Val)
NM_000016.6(ACADM):c.120G>C (p.Glu40Asp)
NM_000016.6(ACADM):c.1211C>T (p.Ser404Leu)
NM_000016.6(ACADM):c.1217T>G (p.Ile406Ser)
NM_000016.6(ACADM):c.154_156del (p.Ala52del) rs2100362599
NM_000016.6(ACADM):c.160A>C (p.Lys54Gln)
NM_000016.6(ACADM):c.17G>A (p.Gly6Glu)
NM_000016.6(ACADM):c.202G>A (p.Asp68Asn) rs2100362891
NM_000016.6(ACADM):c.206A>G (p.Lys69Arg) rs927784210
NM_000016.6(ACADM):c.235AGA[1] (p.Arg80del) rs1553122972
NM_000016.6(ACADM):c.262A>T (p.Asn88Tyr) rs1647171392
NM_000016.6(ACADM):c.265A>C (p.Thr89Pro) rs371194356
NM_000016.6(ACADM):c.286+6C>T
NM_000016.6(ACADM):c.289G>A (p.Gly97Ser) rs1553123053
NM_000016.6(ACADM):c.30+5G>C
NM_000016.6(ACADM):c.302G>A (p.Gly101Glu) rs875989862
NM_000016.6(ACADM):c.307T>C (p.Phe103Leu)
NM_000016.6(ACADM):c.31-12T>G
NM_000016.6(ACADM):c.31-13G>A
NM_000016.6(ACADM):c.31-5T>A
NM_000016.6(ACADM):c.327T>A (p.Ser109Arg) rs1647188135
NM_000016.6(ACADM):c.32T>C (p.Val11Ala)
NM_000016.6(ACADM):c.351_352delinsCA (p.Gly118Arg) rs1553123069
NM_000016.6(ACADM):c.352G>T (p.Gly118Trp)
NM_000016.6(ACADM):c.371A>G (p.Glu124Gly) rs759305231
NM_000016.6(ACADM):c.379T>C (p.Ser127Pro) rs1647189185
NM_000016.6(ACADM):c.380C>A (p.Ser127Tyr)
NM_000016.6(ACADM):c.382T>G (p.Leu128Val)
NM_000016.6(ACADM):c.385G>T (p.Gly129Trp) rs886042076
NM_000016.6(ACADM):c.404T>C (p.Ile135Thr)
NM_000016.6(ACADM):c.455A>G (p.Glu152Gly)
NM_000016.6(ACADM):c.468+11G>A
NM_000016.6(ACADM):c.468+3G>T
NM_000016.6(ACADM):c.468T>G (p.Cys156Trp) rs1647214213
NM_000016.6(ACADM):c.509C>A (p.Ala170Asp)
NM_000016.6(ACADM):c.532A>C (p.Lys178Gln)
NM_000016.6(ACADM):c.576A>G (p.Ile192Met) rs1647482271
NM_000016.6(ACADM):c.598T>C (p.Trp200Arg)
NM_000016.6(ACADM):c.625C>G (p.Pro209Ala) rs765741682
NM_000016.6(ACADM):c.643G>C (p.Ala215Pro)
NM_000016.6(ACADM):c.653C>A (p.Ala218Asp)
NM_000016.6(ACADM):c.656T>G (p.Phe219Cys) rs2100408210
NM_000016.6(ACADM):c.694C>G (p.Gln232Glu) rs2100408490
NM_000016.6(ACADM):c.708+3A>G rs2100408597
NM_000016.6(ACADM):c.708+6G>A rs958629659
NM_000016.6(ACADM):c.725A>G (p.Gln242Arg)
NM_000016.6(ACADM):c.746G>A (p.Gly249Glu) rs1648077584
NM_000016.6(ACADM):c.751G>A (p.Val251Ile)
NM_000016.6(ACADM):c.775A>G (p.Lys259Glu)
NM_000016.6(ACADM):c.77A>C (p.Lys26Thr) rs2100347143
NM_000016.6(ACADM):c.785T>A (p.Val262Asp) rs1489192992
NM_000016.6(ACADM):c.839C>G (p.Thr280Ser)
NM_000016.6(ACADM):c.83A>G (p.Asn28Ser)
NM_000016.6(ACADM):c.863_865dup (p.Ala288_Val289insAla)
NM_000016.6(ACADM):c.865G>T (p.Val289Phe) rs1648137997
NM_000016.6(ACADM):c.87A>G (p.Arg29=) rs2100347177
NM_000016.6(ACADM):c.881_882delinsTT (p.Arg294Ile)
NM_000016.6(ACADM):c.891T>A (p.Asp297Glu)
NM_000016.6(ACADM):c.893_898del (p.Glu298_Thr300delinsAla)
NM_000016.6(ACADM):c.907G>A (p.Ala303Thr) rs875989855
NM_000016.6(ACADM):c.927C>G (p.Phe309Leu) rs771550655
NM_000016.6(ACADM):c.946-2dup rs1648822448
NM_000016.6(ACADM):c.955A>G (p.Ile319Val)
NM_000016.6(ACADM):c.98C>G (p.Pro33Arg)

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