ClinVar Miner

List of variants in gene ARFGEF2 reported as uncertain significance by GeneDx

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_006420.3(ARFGEF2):c.172C>T (p.Pro58Ser) rs149471454 0.00045
NM_006420.3(ARFGEF2):c.5228T>C (p.Met1743Thr) rs367994107 0.00043
NM_006420.3(ARFGEF2):c.3046G>C (p.Gly1016Arg) rs149644732 0.00029
NM_006420.3(ARFGEF2):c.2686-16C>A rs370562126 0.00028
NM_006420.3(ARFGEF2):c.1487G>A (p.Arg496Lys) rs147345525 0.00019
NM_006420.3(ARFGEF2):c.1294A>G (p.Ile432Val) rs41296207 0.00015
NM_006420.3(ARFGEF2):c.493A>G (p.Thr165Ala) rs148230420 0.00014
NM_006420.3(ARFGEF2):c.2010G>A (p.Met670Ile) rs144227832 0.00013
NM_006420.3(ARFGEF2):c.694C>T (p.Arg232Cys) rs200040098 0.00013
NM_006420.3(ARFGEF2):c.4790C>T (p.Thr1597Met) rs368410119 0.00007
NM_006420.3(ARFGEF2):c.5266C>T (p.Arg1756Trp) rs139003168 0.00006
NM_006420.3(ARFGEF2):c.3107T>C (p.Met1036Thr) rs758124206 0.00005
NM_006420.3(ARFGEF2):c.5107G>C (p.Glu1703Gln) rs543611054 0.00005
NM_006420.3(ARFGEF2):c.847G>A (p.Asp283Asn) rs372150935 0.00005
NM_006420.3(ARFGEF2):c.2777G>A (p.Arg926Gln) rs763245062 0.00004
NM_006420.3(ARFGEF2):c.3650A>G (p.Asn1217Ser) rs769315845 0.00004
NM_006420.3(ARFGEF2):c.5024G>A (p.Arg1675His) rs778607741 0.00004
NM_006420.3(ARFGEF2):c.5282G>A (p.Arg1761Gln) rs771293652 0.00004
NM_006420.3(ARFGEF2):c.757G>A (p.Gly253Ser) rs754473579 0.00004
NM_006420.3(ARFGEF2):c.1289A>G (p.Asn430Ser) rs373419435 0.00003
NM_006420.3(ARFGEF2):c.2639C>T (p.Pro880Leu) rs183852730 0.00003
NM_006420.3(ARFGEF2):c.338G>A (p.Arg113Gln) rs143956045 0.00003
NM_006420.3(ARFGEF2):c.5238C>T (p.Asp1746=) rs371687802 0.00003
NM_006420.3(ARFGEF2):c.1958+6T>C rs770037712 0.00001
NM_006420.3(ARFGEF2):c.3034C>T (p.Arg1012Cys) rs758071330 0.00001
NM_006420.3(ARFGEF2):c.4003G>A (p.Glu1335Lys) rs374632843 0.00001
NM_006420.3(ARFGEF2):c.1420A>T (p.Ile474Leu)
NM_006420.3(ARFGEF2):c.1526-3A>G rs2123420984
NM_006420.3(ARFGEF2):c.1979G>C (p.Arg660Thr)
NM_006420.3(ARFGEF2):c.2071-11G>T rs2123452886
NM_006420.3(ARFGEF2):c.2106G>T (p.Arg702Ser) rs1057522261
NM_006420.3(ARFGEF2):c.2407G>T (p.Gly803Cys) rs371043044
NM_006420.3(ARFGEF2):c.2504T>A (p.Leu835Gln) rs2123460032
NM_006420.3(ARFGEF2):c.3023G>A (p.Gly1008Asp) rs763952872
NM_006420.3(ARFGEF2):c.3323C>T (p.Pro1108Leu) rs767791225
NM_006420.3(ARFGEF2):c.3608C>T (p.Ala1203Val)
NM_006420.3(ARFGEF2):c.3790A>G (p.Ile1264Val)
NM_006420.3(ARFGEF2):c.3857C>T (p.Thr1286Met)
NM_006420.3(ARFGEF2):c.4135T>C (p.Phe1379Leu) rs573211337
NM_006420.3(ARFGEF2):c.4219T>C (p.Tyr1407His) rs1319305357
NM_006420.3(ARFGEF2):c.4280A>T (p.Asp1427Val) rs2123534625
NM_006420.3(ARFGEF2):c.4668G>C (p.Gln1556His) rs2123556844
NM_006420.3(ARFGEF2):c.4889C>T (p.Ser1630Phe)
NM_006420.3(ARFGEF2):c.710A>G (p.Gln237Arg) rs2091086629
NM_006420.3(ARFGEF2):c.955G>A (p.Glu319Lys) rs1057523412

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