ClinVar Miner

List of variants in gene combination AIFM1, RAB33A reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_004208.4(AIFM1):c.1156G>A (p.Gly386Ser) rs746155778 0.00005
NM_004208.4(AIFM1):c.1030C>T (p.Leu344Phe) rs184474885 0.00004
NM_004208.4(AIFM1):c.1597G>A (p.Glu533Lys) rs1057517852 0.00004
NM_004208.4(AIFM1):c.952G>A (p.Ala318Thr) rs773680831 0.00003
NM_004208.4(AIFM1):c.1465G>A (p.Asp489Asn) rs748493176 0.00002
NM_004208.4(AIFM1):c.365A>C (p.Glu122Ala) rs2030812042 0.00002
NM_004208.4(AIFM1):c.808A>G (p.Ile270Val) rs1450416950 0.00002
NM_004208.4(AIFM1):c.1049A>T (p.Asn350Ile) rs1189292666 0.00001
NM_004208.4(AIFM1):c.1087G>T (p.Val363Leu) rs894365881 0.00001
NM_004208.4(AIFM1):c.1501A>T (p.Ser501Cys) rs769816388 0.00001
NM_004208.4(AIFM1):c.1534A>G (p.Thr512Ala) rs369259253 0.00001
NM_004208.4(AIFM1):c.1646C>T (p.Ala549Val) rs761953453 0.00001
NM_004208.4(AIFM1):c.452G>A (p.Arg151Gln) rs752742151 0.00001
NM_004208.4(AIFM1):c.602G>A (p.Arg201Lys) rs886703882 0.00001
NM_004208.4(AIFM1):c.646G>A (p.Asp216Asn) rs1170792825 0.00001
NM_004208.4(AIFM1):c.1001T>A (p.Phe334Tyr) rs2523121067
NM_004208.4(AIFM1):c.1006G>A (p.Glu336Lys) rs1603223158
NM_004208.4(AIFM1):c.1020G>T (p.Met340Ile) rs2523120985
NM_004208.4(AIFM1):c.1029C>G (p.Ile343Met) rs2124653028
NM_004208.4(AIFM1):c.1061A>C (p.Glu354Ala) rs2523120787
NM_004208.4(AIFM1):c.1081G>A (p.Val361Ile) rs1569417347
NM_004208.4(AIFM1):c.1090A>G (p.Met364Val) rs1556262326
NM_004208.4(AIFM1):c.1120G>A (p.Val374Ile) rs1057521792
NM_004208.4(AIFM1):c.1171A>G (p.Thr391Ala) rs2523117705
NM_004208.4(AIFM1):c.1181T>C (p.Ile394Thr) rs2523117658
NM_004208.4(AIFM1):c.1183G>C (p.Val395Leu) rs2124651880
NM_004208.4(AIFM1):c.1232G>C (p.Gly411Ala) rs753549726
NM_004208.4(AIFM1):c.1240A>G (p.Ile414Val) rs2124651762
NM_004208.4(AIFM1):c.1343G>A (p.Gly448Glu) rs2523110396
NM_004208.4(AIFM1):c.1435C>G (p.Gln479Glu) rs2124648352
NM_004208.4(AIFM1):c.143_145del (p.Leu48del) rs1227558669
NM_004208.4(AIFM1):c.1465G>C (p.Asp489His)
NM_004208.4(AIFM1):c.1483A>G (p.Ile495Val) rs2030090475
NM_004208.4(AIFM1):c.1495G>T (p.Asp499Tyr) rs2124646080
NM_004208.4(AIFM1):c.1506G>T (p.Leu502Phe) rs2030089803
NM_004208.4(AIFM1):c.1574G>A (p.Gly525Glu) rs1556252472
NM_004208.4(AIFM1):c.1592A>T (p.Glu531Val) rs1285480966
NM_004208.4(AIFM1):c.1607C>T (p.Ser536Phe)
NM_004208.4(AIFM1):c.1619A>C (p.Glu540Ala)
NM_004208.4(AIFM1):c.1636A>G (p.Ser546Gly) rs1569415378
NM_004208.4(AIFM1):c.1720G>T (p.Val574Leu)
NM_004208.4(AIFM1):c.182G>T (p.Gly61Val)
NM_004208.4(AIFM1):c.262A>C (p.Met88Leu)
NM_004208.4(AIFM1):c.347C>G (p.Ser116Cys)
NM_004208.4(AIFM1):c.374A>C (p.Gln125Pro) rs2124664648
NM_004208.4(AIFM1):c.402C>A (p.Phe134Leu) rs2523146566
NM_004208.4(AIFM1):c.451C>T (p.Arg151Trp)
NM_004208.4(AIFM1):c.460G>A (p.Asp154Asn) rs999882329
NM_004208.4(AIFM1):c.497C>T (p.Pro166Leu) rs193920813
NM_004208.4(AIFM1):c.548A>G (p.Asp183Gly)
NM_004208.4(AIFM1):c.646G>T (p.Asp216Tyr)
NM_004208.4(AIFM1):c.673G>A (p.Val225Met) rs2523140736
NM_004208.4(AIFM1):c.754A>C (p.Thr252Pro)
NM_004208.4(AIFM1):c.790C>G (p.Pro264Ala) rs2523129670
NM_004208.4(AIFM1):c.910A>G (p.Thr304Ala)
NM_004208.4(AIFM1):c.910A>T (p.Thr304Ser) rs2124655204
NM_004208.4(AIFM1):c.925G>A (p.Gly309Ser)

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