ClinVar Miner

List of variants in gene BRAT1 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 119
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HGVS dbSNP gnomAD frequency
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932 0.00249
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp) rs61753094 0.00152
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val) rs140833277 0.00095
NM_152743.4(BRAT1):c.1792C>T (p.His598Tyr) rs201523118 0.00088
NM_152743.4(BRAT1):c.1564G>C (p.Glu522Gln) rs145509776 0.00083
NM_152743.4(BRAT1):c.2041G>A (p.Glu681Lys) rs145833100 0.00079
NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser) rs147745609 0.00078
NM_152743.4(BRAT1):c.2147C>T (p.Ala716Val) rs140802292 0.00075
NM_152743.4(BRAT1):c.826G>A (p.Asp276Asn) rs146546197 0.00070
NM_152743.4(BRAT1):c.924-6C>G rs376179903 0.00063
NM_152743.4(BRAT1):c.2029G>A (p.Val677Met) rs141726264 0.00043
NM_152743.4(BRAT1):c.883A>G (p.Met295Val) rs151317339 0.00038
NM_152743.4(BRAT1):c.1727G>C (p.Gly576Ala) rs150846882 0.00035
NM_152743.4(BRAT1):c.1972G>A (p.Ala658Thr) rs186448943 0.00030
NM_152743.4(BRAT1):c.1421C>T (p.Thr474Met) rs148923187 0.00029
NM_152743.4(BRAT1):c.1594G>A (p.Gly532Arg) rs142129866 0.00028
NM_152743.4(BRAT1):c.871G>A (p.Gly291Ser) rs764583480 0.00023
NM_152743.4(BRAT1):c.2340C>G (p.Asp780Glu) rs201045158 0.00021
NM_152743.4(BRAT1):c.424G>A (p.Asp142Asn) rs183545975 0.00019
NM_152743.4(BRAT1):c.1087G>A (p.Gly363Ser) rs967919052 0.00016
NM_152743.4(BRAT1):c.763G>A (p.Ala255Thr) rs149503475 0.00016
NM_152743.4(BRAT1):c.1318A>T (p.Thr440Ser) rs141751133 0.00015
NM_152743.4(BRAT1):c.626C>T (p.Ala209Val) rs112960104 0.00013
NM_152743.4(BRAT1):c.2009G>A (p.Arg670His) rs147119058 0.00011
NM_152743.4(BRAT1):c.1451C>G (p.Thr484Ser) rs200248064 0.00010
NM_152743.4(BRAT1):c.679C>T (p.Arg227Cys) rs79263074 0.00010
NM_152743.4(BRAT1):c.1656G>C (p.Gln552His) rs376177219 0.00009
NM_152743.4(BRAT1):c.2321C>T (p.Ala774Val) rs372230882 0.00009
NM_152743.4(BRAT1):c.2329A>G (p.Arg777Gly) rs773571503 0.00009
NM_152743.4(BRAT1):c.1340C>T (p.Thr447Met) rs368808380 0.00008
NM_152743.4(BRAT1):c.1487A>G (p.Gln496Arg) rs142667367 0.00008
NM_152743.4(BRAT1):c.1046C>T (p.Thr349Met) rs112658000 0.00007
NM_152743.4(BRAT1):c.1304C>T (p.Thr435Met) rs745563920 0.00007
NM_152743.4(BRAT1):c.1357C>T (p.Leu453Phe) rs760510041 0.00007
NM_152743.4(BRAT1):c.1484C>T (p.Pro495Leu) rs577945739 0.00007
NM_152743.4(BRAT1):c.1039G>A (p.Asp347Asn) rs144499760 0.00006
NM_152743.4(BRAT1):c.1061T>A (p.Leu354His) rs999376070 0.00006
NM_152743.4(BRAT1):c.1879G>A (p.Ala627Thr) rs750400556 0.00006
NM_152743.4(BRAT1):c.2360C>T (p.Thr787Met) rs375916445 0.00006
NM_152743.4(BRAT1):c.2449G>A (p.Glu817Lys) rs761588914 0.00006
NM_152743.4(BRAT1):c.1134+3A>G rs200692755 0.00005
NM_152743.4(BRAT1):c.1177G>A (p.Ala393Thr) rs35659709 0.00005
NM_152743.4(BRAT1):c.578C>T (p.Ala193Val) rs144841598 0.00005
NM_152743.4(BRAT1):c.59G>A (p.Arg20Lys) rs143390199 0.00005
NM_152743.4(BRAT1):c.1618G>A (p.Ala540Thr) rs148608404 0.00004
NM_152743.4(BRAT1):c.1702G>A (p.Ala568Thr) rs141709461 0.00004
NM_152743.4(BRAT1):c.1765C>T (p.Arg589Trp) rs141490198 0.00004
NM_152743.4(BRAT1):c.2003C>T (p.Pro668Leu) rs758503229 0.00004
NM_152743.4(BRAT1):c.2089C>T (p.His697Tyr) rs561549620 0.00004
NM_152743.4(BRAT1):c.680G>A (p.Arg227His) rs911372208 0.00004
NM_152743.4(BRAT1):c.851C>T (p.Ala284Val) rs750645922 0.00004
NM_152743.4(BRAT1):c.1100G>A (p.Arg367His) rs774408317 0.00003
NM_152743.4(BRAT1):c.1163C>T (p.Ala388Val) rs368710298 0.00003
NM_152743.4(BRAT1):c.139G>A (p.Val47Met) rs769700664 0.00003
NM_152743.4(BRAT1):c.1804G>A (p.Val602Ile) rs532881368 0.00003
NM_152743.4(BRAT1):c.346G>A (p.Val116Ile) rs750543404 0.00003
NM_152743.4(BRAT1):c.349C>T (p.Pro117Ser) rs767516238 0.00003
NM_152743.4(BRAT1):c.382C>T (p.Arg128Cys) rs770461144 0.00003
NM_152743.4(BRAT1):c.811G>A (p.Val271Met) rs746527927 0.00003
NM_152743.4(BRAT1):c.920A>C (p.His307Pro) rs778881636 0.00003
NM_152743.4(BRAT1):c.1351G>A (p.Ala451Thr) rs138276986 0.00002
NM_152743.4(BRAT1):c.1522C>T (p.Arg508Cys) rs751548415 0.00002
NM_152743.4(BRAT1):c.2092G>A (p.Val698Met) rs781355172 0.00002
NM_152743.4(BRAT1):c.652C>G (p.Leu218Val) rs1471856951 0.00002
NM_152743.4(BRAT1):c.802C>T (p.Arg268Cys) rs145047426 0.00002
NM_152743.4(BRAT1):c.844A>T (p.Thr282Ser) rs575570226 0.00002
NM_152743.4(BRAT1):c.1129C>T (p.Pro377Ser) rs780327501 0.00001
NM_152743.4(BRAT1):c.1135-4G>A rs1404214519 0.00001
NM_152743.4(BRAT1):c.1280G>A (p.Arg427Gln) rs375466838 0.00001
NM_152743.4(BRAT1):c.1354G>C (p.Val452Leu) rs1223186309 0.00001
NM_152743.4(BRAT1):c.1384T>C (p.Ser462Pro) rs761704986 0.00001
NM_152743.4(BRAT1):c.1521A>C (p.Lys507Asn) rs1442646274 0.00001
NM_152743.4(BRAT1):c.158C>G (p.Pro53Arg) rs368397368 0.00001
NM_152743.4(BRAT1):c.1819T>A (p.Phe607Ile) rs564013530 0.00001
NM_152743.4(BRAT1):c.1873G>A (p.Ala625Thr) rs758308165 0.00001
NM_152743.4(BRAT1):c.1954G>A (p.Ala652Thr) rs772861328 0.00001
NM_152743.4(BRAT1):c.389T>C (p.Leu130Pro) rs1234481462 0.00001
NM_152743.4(BRAT1):c.400C>T (p.Pro134Ser) rs1250652407 0.00001
NM_152743.4(BRAT1):c.575C>T (p.Pro192Leu) rs772270013 0.00001
NM_152743.4(BRAT1):c.853C>T (p.Arg285Trp) rs1301692811 0.00001
NM_152743.4(BRAT1):c.1012C>T (p.Pro338Ser) rs373020561
NM_152743.4(BRAT1):c.113C>T (p.Thr38Met) rs1780250788
NM_152743.4(BRAT1):c.1186A>T (p.Thr396Ser)
NM_152743.4(BRAT1):c.1211C>T (p.Ser404Leu)
NM_152743.4(BRAT1):c.1252A>T (p.Thr418Ser) rs202145442
NM_152743.4(BRAT1):c.1267G>A (p.Val423Ile) rs141807337
NM_152743.4(BRAT1):c.1288C>T (p.Leu430Phe)
NM_152743.4(BRAT1):c.1312C>G (p.Gln438Glu)
NM_152743.4(BRAT1):c.1346C>T (p.Ala449Val) rs747980905
NM_152743.4(BRAT1):c.1394C>T (p.Thr465Met) rs1021569403
NM_152743.4(BRAT1):c.1472G>C (p.Gly491Ala) rs762040027
NM_152743.4(BRAT1):c.1564G>A (p.Glu522Lys) rs145509776
NM_152743.4(BRAT1):c.1766G>A (p.Arg589Gln) rs375281590
NM_152743.4(BRAT1):c.1866C>A (p.Asp622Glu) rs371142628
NM_152743.4(BRAT1):c.2137C>T (p.Arg713Cys)
NM_152743.4(BRAT1):c.2298C>A (p.Asp766Glu) rs144085416
NM_152743.4(BRAT1):c.2311G>T (p.Ala771Ser)
NM_152743.4(BRAT1):c.23T>G (p.Leu8Arg)
NM_152743.4(BRAT1):c.2416A>G (p.Met806Val)
NM_152743.4(BRAT1):c.2453C>T (p.Ala818Val) rs1778817640
NM_152743.4(BRAT1):c.2455G>A (p.Asp819Asn) rs766501904
NM_152743.4(BRAT1):c.249C>A (p.Phe83Leu) rs1339437631
NM_152743.4(BRAT1):c.334G>A (p.Ala112Thr)
NM_152743.4(BRAT1):c.350C>G (p.Pro117Arg) rs2128399658
NM_152743.4(BRAT1):c.364G>T (p.Gly122Cys) rs368753862
NM_152743.4(BRAT1):c.393_422del (p.Gln132_Ala141del) rs1562582216
NM_152743.4(BRAT1):c.393_422dup (p.Gln132_Ala141dup) rs1562582216
NM_152743.4(BRAT1):c.437T>A (p.Val146Asp) rs778638400
NM_152743.4(BRAT1):c.439G>A (p.Asp147Asn)
NM_152743.4(BRAT1):c.522G>C (p.Leu174Phe) rs2128397295
NM_152743.4(BRAT1):c.545G>A (p.Gly182Glu) rs148598276
NM_152743.4(BRAT1):c.597_598delinsTT (p.Met199_Asp200delinsIleTyr) rs1583311462
NM_152743.4(BRAT1):c.764C>T (p.Ala255Val) rs1779355816
NM_152743.4(BRAT1):c.781G>C (p.Asp261His)
NM_152743.4(BRAT1):c.803G>T (p.Arg268Leu)
NM_152743.4(BRAT1):c.814T>C (p.Phe272Leu) rs1562577958
NM_152743.4(BRAT1):c.957C>A (p.Val319=) rs1779227281
NM_152743.4(BRAT1):c.983T>C (p.Leu328Pro) rs1291695271
NM_152743.4(BRAT1):c.988_989delinsAA (p.Ala330Asn) rs1779222833

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