ClinVar Miner

List of variants in gene RAB3GAP2 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_012414.4(RAB3GAP2):c.3924G>C (p.Thr1308=) rs73098539 0.00338
NM_012414.4(RAB3GAP2):c.4060A>G (p.Ile1354Val) rs59190330 0.00174
NM_012414.4(RAB3GAP2):c.39C>T (p.Asp13=) rs145667920 0.00136
NM_012414.4(RAB3GAP2):c.938C>T (p.Thr313Ile) rs74139292 0.00104
NM_012414.4(RAB3GAP2):c.2290C>T (p.Leu764Phe) rs139337049 0.00097
NM_012414.4(RAB3GAP2):c.112C>T (p.Pro38Ser) rs138796052 0.00096
NM_012414.4(RAB3GAP2):c.3867+13C>T rs200579008 0.00087
NM_012414.4(RAB3GAP2):c.3842A>G (p.Tyr1281Cys) rs34081806 0.00084
NM_012414.4(RAB3GAP2):c.3991C>A (p.Leu1331Ile) rs149842844 0.00050
NM_012414.4(RAB3GAP2):c.3390G>A (p.Ala1130=) rs140377995 0.00046
NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu) rs150643803 0.00044
NM_012414.4(RAB3GAP2):c.3337-6C>T rs137894782 0.00020
NM_012414.4(RAB3GAP2):c.1580C>T (p.Pro527Leu) rs149563712 0.00019
NM_012414.4(RAB3GAP2):c.2304G>A (p.Leu768=) rs140146408 0.00014
NM_012414.4(RAB3GAP2):c.3143A>G (p.His1048Arg) rs151244742 0.00013
NM_012414.4(RAB3GAP2):c.2946A>G (p.Val982=) rs748154558 0.00012
NM_012414.4(RAB3GAP2):c.1215C>T (p.Phe405=) rs762485949 0.00009
NM_012414.4(RAB3GAP2):c.1281C>T (p.Asp427=) rs372594666 0.00006
NM_012414.4(RAB3GAP2):c.1709A>G (p.Asn570Ser) rs143286302 0.00006
NM_012414.4(RAB3GAP2):c.2282C>T (p.Ser761Leu) rs562096116 0.00006
NM_012414.4(RAB3GAP2):c.3558A>G (p.Gly1186=) rs543785834 0.00004
NM_012414.4(RAB3GAP2):c.1584G>A (p.Val528=) rs372216761 0.00003
NM_012414.4(RAB3GAP2):c.2417-4A>G rs577016598 0.00003
NM_012414.4(RAB3GAP2):c.2607A>G (p.Ser869=) rs1658167378 0.00001
NM_012414.4(RAB3GAP2):c.304+15A>G rs771063121 0.00001
NM_012414.4(RAB3GAP2):c.3945G>A (p.Ala1315=) rs778048062 0.00001
NM_012414.4(RAB3GAP2):c.1231T>C (p.Leu411=) rs2528685183
NM_012414.4(RAB3GAP2):c.2091dup (p.Val698fs) rs2528663434
NM_012414.4(RAB3GAP2):c.3400G>C (p.Val1134Leu) rs138489010

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