ClinVar Miner

List of variants in gene BRAT1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 98
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HGVS dbSNP gnomAD frequency
NM_152743.4(BRAT1):c.924-236C>T rs77542618 0.02825
NM_152743.4(BRAT1):c.282+141A>C rs12666641 0.02107
NM_152743.4(BRAT1):c.1206C>T (p.Asp402=) rs7807895 0.01413
NM_152743.4(BRAT1):c.1598-57C>T rs116570394 0.01185
NM_152743.4(BRAT1):c.283-75G>A rs144804514 0.01182
NM_152743.4(BRAT1):c.*219C>A rs145828184 0.01166
NM_152743.4(BRAT1):c.1395+119G>T rs75654424 0.01153
NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser) rs77015302 0.01031
NM_152743.4(BRAT1):c.127+246C>T rs61200904 0.00971
NM_152743.4(BRAT1):c.1135-8C>A rs113613637 0.00936
NM_152743.4(BRAT1):c.1015+70A>G rs115083971 0.00916
NM_152743.4(BRAT1):c.431-104T>C rs144673038 0.00904
NM_152743.4(BRAT1):c.127+235C>T rs11981084 0.00876
NM_152743.4(BRAT1):c.1396-120C>G rs141407073 0.00845
NM_152743.4(BRAT1):c.-16-289C>G rs144558259 0.00836
NM_152743.4(BRAT1):c.-16-268T>G rs148689602 0.00710
NM_152743.4(BRAT1):c.*14C>T rs140062589 0.00709
NM_152743.4(BRAT1):c.962T>G (p.Leu321Arg) rs150942467 0.00675
NM_152743.4(BRAT1):c.-16-66G>A rs112496091 0.00656
NM_152743.4(BRAT1):c.282+139G>A rs112866896 0.00652
NM_152743.4(BRAT1):c.1884C>T (p.Ala628=) rs142346283 0.00625
NM_152743.4(BRAT1):c.866G>C (p.Cys289Ser) rs140451075 0.00598
NM_152743.4(BRAT1):c.1396-206G>C rs183241194 0.00594
NM_152743.4(BRAT1):c.803+11C>T rs150359205 0.00551
NM_152743.4(BRAT1):c.431-200G>T rs148497258 0.00546
NM_152743.4(BRAT1):c.1134+71C>T rs77611174 0.00504
NM_152743.4(BRAT1):c.283-239G>A rs151307068 0.00501
NM_152743.4(BRAT1):c.283-232G>A rs190068402 0.00496
NM_152743.4(BRAT1):c.675C>T (p.Phe225=) rs139443843 0.00438
NM_152743.4(BRAT1):c.803+125G>A rs77555101 0.00430
NM_152743.4(BRAT1):c.1770+57G>A rs78571691 0.00426
NM_152743.4(BRAT1):c.1016-135G>A rs77404322 0.00407
NM_152743.4(BRAT1):c.1689G>A (p.Ala563=) rs146276208 0.00310
NM_152743.4(BRAT1):c.1922C>T (p.Ala641Val) rs113030000 0.00206
NM_152743.4(BRAT1):c.1659C>T (p.Leu553=) rs61746940 0.00205
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616 0.00198
NM_152743.4(BRAT1):c.2208G>T (p.Leu736=) rs61753093 0.00159
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp) rs61753094 0.00152
NM_152743.4(BRAT1):c.728G>A (p.Arg243His) rs148261595 0.00152
NM_152743.4(BRAT1):c.1579C>T (p.Leu527=) rs151161353 0.00126
NM_152743.4(BRAT1):c.1015+27G>T rs370805422 0.00103
NM_152743.4(BRAT1):c.1597+36C>T rs200635453 0.00098
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val) rs140833277 0.00095
NM_152743.4(BRAT1):c.1322-12C>T rs200963118 0.00093
NM_152743.4(BRAT1):c.361A>C (p.Ser121Arg) rs138585448 0.00091
NM_152743.4(BRAT1):c.1792C>T (p.His598Tyr) rs201523118 0.00088
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.825C>T (p.Ser275=) rs141320181 0.00067
NM_152743.4(BRAT1):c.431G>A (p.Gly144Asp) rs199745325 0.00036
NM_152743.4(BRAT1):c.955G>A (p.Val319Ile) rs140903769 0.00034
NM_152743.4(BRAT1):c.1594G>A (p.Gly532Arg) rs142129866 0.00028
NM_152743.4(BRAT1):c.2259G>A (p.Pro753=) rs376271902 0.00023
NM_152743.4(BRAT1):c.1396-11A>G rs200500603 0.00021
NM_152743.4(BRAT1):c.1701C>T (p.Thr567=) rs199766692 0.00016
NM_152743.4(BRAT1):c.354C>T (p.Thr118=) rs148913309 0.00014
NM_152743.4(BRAT1):c.762C>T (p.Pro254=) rs143192367 0.00014
NM_152743.4(BRAT1):c.1941C>T (p.Asp647=) rs376101375 0.00013
NM_152743.4(BRAT1):c.1164G>A (p.Ala388=) rs201141165 0.00011
NM_152743.4(BRAT1):c.2004G>A (p.Pro668=) rs368232132 0.00009
NM_152743.4(BRAT1):c.576C>T (p.Pro192=) rs374294371 0.00009
NM_152743.4(BRAT1):c.328G>A (p.Gly110Ser) rs751198409 0.00008
NM_152743.4(BRAT1):c.1032G>A (p.Thr344=) rs371220513 0.00006
NM_152743.4(BRAT1):c.1498+6G>A rs758246723 0.00006
NM_152743.4(BRAT1):c.1791G>A (p.Leu597=) rs759517314 0.00006
NM_152743.4(BRAT1):c.657C>T (p.Asn219=) rs143559840 0.00005
NM_152743.4(BRAT1):c.2361G>A (p.Thr787=) rs757243199 0.00004
NM_152743.4(BRAT1):c.570C>T (p.Asp190=) rs745728832 0.00004
NM_152743.4(BRAT1):c.909G>A (p.Leu303=) rs61742752 0.00004
NM_152743.4(BRAT1):c.1620A>G (p.Ala540=) rs762496445 0.00003
NM_152743.4(BRAT1):c.2052A>G (p.Pro684=) rs775271322 0.00003
NM_152743.4(BRAT1):c.2148G>A (p.Ala716=) rs756583395 0.00003
NM_152743.4(BRAT1):c.2448C>T (p.Asp816=) rs200784213 0.00003
NM_152743.4(BRAT1):c.2454C>T (p.Ala818=) rs557088612 0.00003
NM_152743.4(BRAT1):c.474G>A (p.Leu158=) rs141198732 0.00003
NM_152743.4(BRAT1):c.1146T>A (p.Pro382=) rs763005854 0.00002
NM_152743.4(BRAT1):c.1152G>A (p.Pro384=) rs185653171 0.00002
NM_152743.4(BRAT1):c.2088C>T (p.Cys696=) rs369595259 0.00002
NM_152743.4(BRAT1):c.669G>A (p.Thr223=) rs781646381 0.00002
NM_152743.4(BRAT1):c.852G>A (p.Ala284=) rs767671540 0.00002
NM_152743.4(BRAT1):c.2133C>T (p.Cys711=) rs149690979 0.00001
NM_152743.4(BRAT1):c.2367C>T (p.Ala789=) rs200892967 0.00001
NM_152743.4(BRAT1):c.2377G>A (p.Asp793Asn) rs759036645 0.00001
NM_152743.4(BRAT1):c.*10G>C rs190232808
NM_152743.4(BRAT1):c.117C>T (p.Val39=)
NM_152743.4(BRAT1):c.128-276_128-275del rs201970214
NM_152743.4(BRAT1):c.1305G>T (p.Thr435=) rs145506790
NM_152743.4(BRAT1):c.1464T>G (p.Ser488=)
NM_152743.4(BRAT1):c.166G>A (p.Val56Met) rs148548421
NM_152743.4(BRAT1):c.1671T>G (p.Pro557=) rs1583293696
NM_152743.4(BRAT1):c.186G>C (p.Val62=) rs754650421
NM_152743.4(BRAT1):c.2169T>A (p.Leu723=) rs150300694
NM_152743.4(BRAT1):c.2169T>C (p.Leu723=) rs150300694
NM_152743.4(BRAT1):c.2283C>G (p.Ala761=)
NM_152743.4(BRAT1):c.511G>C (p.Val171Leu) rs769663853
NM_152743.4(BRAT1):c.566G>T (p.Gly189Val) rs531827528
NM_152743.4(BRAT1):c.714G>A (p.Val238=) rs1562578908
NM_152743.4(BRAT1):c.729C>T (p.Arg243=) rs770100854

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