ClinVar Miner

List of variants in gene ARFGEF2 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_006420.3(ARFGEF2):c.839-20A>G rs2295031 0.38231
NM_006420.3(ARFGEF2):c.3663T>C (p.Gly1221=) rs2295580 0.38170
NM_006420.3(ARFGEF2):c.4755+19A>G rs7270848 0.36848
NM_006420.3(ARFGEF2):c.2277-16G>A rs4810905 0.23578
NM_006420.3(ARFGEF2):c.4131C>T (p.Ile1377=) rs2281582 0.13125
NM_006420.3(ARFGEF2):c.424-16C>T rs41304647 0.04427
NM_006420.3(ARFGEF2):c.169C>T (p.Pro57Ser) rs73113975 0.00540
NM_006420.3(ARFGEF2):c.1512G>A (p.Thr504=) rs116550473 0.00395
NM_006420.3(ARFGEF2):c.3892G>A (p.Gly1298Ser) rs139037316 0.00124
NM_006420.3(ARFGEF2):c.1888G>A (p.Val630Ile) rs146772848 0.00107
NM_006420.3(ARFGEF2):c.811C>G (p.Pro271Ala) rs143570842 0.00102
NM_006420.3(ARFGEF2):c.1644G>A (p.Glu548=) rs147534008 0.00098
NM_006420.3(ARFGEF2):c.1398T>C (p.Phe466=) rs141596938 0.00081
NM_006420.3(ARFGEF2):c.1947C>T (p.His649=) rs140520386 0.00068
NM_006420.3(ARFGEF2):c.3129G>T (p.Leu1043Phe) rs148770948 0.00063
NM_006420.3(ARFGEF2):c.756C>T (p.Asn252=) rs114729625 0.00031
NM_006420.3(ARFGEF2):c.2553G>A (p.Gln851=) rs201238132 0.00014
NM_006420.3(ARFGEF2):c.4812G>A (p.Lys1604=) rs142036030 0.00014
NM_006420.3(ARFGEF2):c.1329C>T (p.Asn443=) rs192383756 0.00012
NM_006420.3(ARFGEF2):c.1953C>T (p.Ile651=) rs377322572 0.00011
NM_006420.3(ARFGEF2):c.3840C>T (p.Asn1280=) rs371088382 0.00009
NM_006420.3(ARFGEF2):c.2276+6C>T rs368941506 0.00008
NM_006420.3(ARFGEF2):c.2276+10G>A rs376568632 0.00007
NM_006420.3(ARFGEF2):c.3003C>T (p.Leu1001=) rs752737205 0.00006
NM_006420.3(ARFGEF2):c.4212C>T (p.His1404=) rs376257322 0.00004
NM_006420.3(ARFGEF2):c.4625-4A>G rs543559398 0.00002
NM_006420.3(ARFGEF2):c.1203G>A (p.Leu401=) rs747567218 0.00001
NM_006420.3(ARFGEF2):c.*2C>G
NM_006420.3(ARFGEF2):c.1026T>C (p.Asp342=)
NM_006420.3(ARFGEF2):c.1228C>T (p.Leu410=)
NM_006420.3(ARFGEF2):c.1852A>G (p.Met618Val)
NM_006420.3(ARFGEF2):c.2319G>A (p.Ala773=)
NM_006420.3(ARFGEF2):c.2362-9dup
NM_006420.3(ARFGEF2):c.276+6A>G rs1427216608
NM_006420.3(ARFGEF2):c.3177G>T (p.Ser1059=) rs61748373
NM_006420.3(ARFGEF2):c.3195G>A (p.Ser1065=)
NM_006420.3(ARFGEF2):c.3758-3del rs797045256
NM_006420.3(ARFGEF2):c.4120C>T (p.Leu1374=)
NM_006420.3(ARFGEF2):c.4456T>C (p.Leu1486=)
NM_006420.3(ARFGEF2):c.4620C>T (p.Tyr1540=)
NM_006420.3(ARFGEF2):c.4756-7C>T rs868504867
NM_006420.3(ARFGEF2):c.4791G>A (p.Thr1597=)
NM_006420.3(ARFGEF2):c.5352G>A (p.Val1784=)
NM_006420.3(ARFGEF2):c.573C>T (p.Asn191=)
NM_006420.3(ARFGEF2):c.849C>T (p.Asp283=)

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