ClinVar Miner

List of variants in gene RASA2 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_006506.5(RASA2):c.2160= (p.Leu720=) rs295323 0.52396
NM_006506.5(RASA2):c.2016T>C (p.Asn672=) rs295322 0.12892
NM_006506.5(RASA2):c.2519+10T>G rs295324 0.06624
NM_006506.5(RASA2):c.528-19C>T rs75293937 0.02143
NM_006506.5(RASA2):c.2226-5C>T rs112582979 0.00714
NM_006506.5(RASA2):c.1603A>G (p.Ile535Val) rs143035190 0.00283
NM_006506.5(RASA2):c.1020+20G>A rs113251297 0.00222
NM_006506.5(RASA2):c.761+8C>T rs143073468 0.00155
NM_006506.5(RASA2):c.252-18C>G rs184922882 0.00143
NM_006506.5(RASA2):c.2514G>C (p.Gly838=) rs114158487 0.00086
NM_006506.5(RASA2):c.2215C>G (p.Pro739Ala) rs201360260 0.00076
NM_006506.5(RASA2):c.2163C>T (p.Asn721=) rs144508155 0.00065
NM_006506.5(RASA2):c.378A>C (p.Glu126Asp) rs144759014 0.00045
NM_006506.5(RASA2):c.540C>T (p.Cys180=) rs148503095 0.00039
NM_006506.5(RASA2):c.2493A>G (p.Arg831=) rs142634033 0.00026
NM_006506.5(RASA2):c.1826+20C>T rs373342734 0.00020
NM_006506.5(RASA2):c.528-4T>G rs201832322 0.00019
NM_006506.5(RASA2):c.1960G>A (p.Val654Ile) rs150847466 0.00016
NM_006506.5(RASA2):c.1422C>T (p.Cys474=) rs137996961 0.00012
NM_006506.5(RASA2):c.1641T>C (p.Thr547=) rs148158856 0.00011
NM_006506.5(RASA2):c.1674+16T>A rs769778924 0.00009
NM_006506.5(RASA2):c.382T>C (p.Leu128=) rs193019405 0.00009
NM_006506.5(RASA2):c.156A>G (p.Pro52=) rs143703190 0.00007
NM_006506.5(RASA2):c.1942G>A (p.Ala648Thr) rs769395361 0.00006
NM_006506.5(RASA2):c.519T>C (p.Leu173=) rs956512674 0.00006
NM_006506.5(RASA2):c.2226A>T (p.Ala742=) rs754617499 0.00005
NM_006506.5(RASA2):c.2337T>C (p.Cys779=) rs576697395 0.00005
NM_006506.5(RASA2):c.2400C>T (p.Ile800=) rs144565084 0.00004
NM_006506.5(RASA2):c.615T>C (p.Asn205=) rs767353410 0.00004
NM_006506.5(RASA2):c.656C>T (p.Pro219Leu) rs944578775 0.00004
NM_006506.5(RASA2):c.717C>T (p.Ser239=) rs183729614 0.00004
NM_006506.5(RASA2):c.1314C>T (p.Ile438=) rs751326898 0.00003
NM_006506.5(RASA2):c.1216C>T (p.Leu406=) rs146956359 0.00002
NM_006506.5(RASA2):c.255A>G (p.Pro85=) rs768464571 0.00002
NM_006506.5(RASA2):c.1449T>C (p.Tyr483=) rs772636003 0.00001
NM_006506.5(RASA2):c.1886G>A (p.Arg629Gln) rs1469875156 0.00001
NM_006506.5(RASA2):c.2225C>T (p.Ala742Val) rs774848188 0.00001
NM_006506.5(RASA2):c.2329+7A>G rs1444704196 0.00001
NM_006506.5(RASA2):c.792C>G (p.Val264=) rs771687765 0.00001
NM_006506.5(RASA2):c.847T>G (p.Ser283Ala) rs186067272 0.00001
NM_006506.5(RASA2):c.863+13C>A rs776517254 0.00001
NM_006506.5(RASA2):c.1116T>A (p.Asp372Glu) rs2082919565
NM_006506.5(RASA2):c.1126C>T (p.Pro376Ser)
NM_006506.5(RASA2):c.1170-8T>C
NM_006506.5(RASA2):c.1382_1479dup (p.Pro494delinsThrSerTyrSerIleGlnLeuTer) rs2082966552
NM_006506.5(RASA2):c.1410A>G (p.Ser470=)
NM_006506.5(RASA2):c.1483+7G>A
NM_006506.5(RASA2):c.1484-4G>A
NM_006506.5(RASA2):c.1548C>T (p.Ala516=)
NM_006506.5(RASA2):c.1549G>T (p.Val517Leu) rs201190266
NM_006506.5(RASA2):c.1577G>A (p.Arg526Gln)
NM_006506.5(RASA2):c.1580C>T (p.Pro527Leu) rs2083025042
NM_006506.5(RASA2):c.1660C>G (p.Leu554Val)
NM_006506.5(RASA2):c.1675-7T>G rs2107770441
NM_006506.5(RASA2):c.1751_1752+2delinsGGG
NM_006506.5(RASA2):c.1751del (p.Lys584fs)
NM_006506.5(RASA2):c.1752+2T>G
NM_006506.5(RASA2):c.1934-10dup rs1560066820
NM_006506.5(RASA2):c.2020_2021insAT (p.Phe674fs) rs2107801496
NM_006506.5(RASA2):c.2124A>T (p.Gln708His) rs61750362
NM_006506.5(RASA2):c.2129G>A (p.Arg710Lys) rs2083586079
NM_006506.5(RASA2):c.2205C>T (p.Leu735=) rs1029424231
NM_006506.5(RASA2):c.2226-39_2226-17dup rs2083600348
NM_006506.5(RASA2):c.2230G>T (p.Val744Phe) rs1463774211
NM_006506.5(RASA2):c.2330-13C>T
NM_006506.5(RASA2):c.2330-2A>G
NM_006506.5(RASA2):c.2469T>G (p.Pro823=) rs2107803362
NM_006506.5(RASA2):c.248T>G (p.Leu83Ter)
NM_006506.5(RASA2):c.2519+18T>G rs2083613884
NM_006506.5(RASA2):c.2546C>T (p.Ser849Phe)
NM_006506.5(RASA2):c.286C>A (p.Pro96Thr) rs761761007
NM_006506.5(RASA2):c.299A>G (p.Gln100Arg) rs1235489668
NM_006506.5(RASA2):c.356-15A>C rs772907849
NM_006506.5(RASA2):c.374A>G (p.Lys125Arg)
NM_006506.5(RASA2):c.374_443dup (p.Glu148_Val149insArgArgLeuValTer) rs2082232970
NM_006506.5(RASA2):c.527+15dup rs562128860
NM_006506.5(RASA2):c.535G>A (p.Ala179Thr)
NM_006506.5(RASA2):c.610A>G (p.Arg204Gly)
NM_006506.5(RASA2):c.618C>T (p.Asp206=) rs1560029184
NM_006506.5(RASA2):c.657G>A (p.Pro219=) rs34238772
NM_006506.5(RASA2):c.684+15dup rs769572165
NM_006506.5(RASA2):c.882A>G (p.Arg294=) rs2082908209
NM_006506.5(RASA2):c.932_934del (p.Leu311_Asn312delinsTyr) rs2082909407

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