ClinVar Miner

List of variants in gene RREB1 reported as likely benign by Invitae

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Gene type:
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Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_001003699.4(RREB1):c.2905C>T (p.Pro969Ser) rs114810122 0.00237
NM_001003699.4(RREB1):c.3422C>G (p.Pro1141Arg) rs201520366 0.00226
NM_001003699.4(RREB1):c.3404G>T (p.Ser1135Ile) rs116295722 0.00188
NM_001003699.4(RREB1):c.136C>T (p.Pro46Ser) rs141007836 0.00131
NM_001003699.4(RREB1):c.2899G>A (p.Glu967Lys) rs114995726 0.00123
NM_001003699.4(RREB1):c.1717G>A (p.Ala573Thr) rs200949048 0.00111
NM_001003699.4(RREB1):c.5087C>T (p.Pro1696Leu) rs148224708 0.00089
NM_001003699.4(RREB1):c.553C>A (p.Pro185Thr) rs115318121 0.00087
NM_001003699.4(RREB1):c.1217G>A (p.Cys406Tyr) rs115374113 0.00086
NM_001003699.4(RREB1):c.1375A>G (p.Ile459Val) rs199565690 0.00083
NM_001003699.4(RREB1):c.4151G>A (p.Arg1384His) rs34964470 0.00079
NM_001003699.4(RREB1):c.2690A>G (p.Asn897Ser) rs139625876 0.00063
NM_001003699.4(RREB1):c.1842C>G (p.Ile614Met) rs146678576 0.00060
NM_001003699.4(RREB1):c.2958C>T (p.Ser986=) rs61731494 0.00060
NM_001003699.4(RREB1):c.996T>C (p.Ala332=) rs146024995 0.00046
NM_001003699.4(RREB1):c.129C>T (p.Pro43=) rs139982275 0.00043
NM_001003699.4(RREB1):c.2271G>C (p.Leu757=) rs144788619 0.00043
NM_001003699.4(RREB1):c.2152C>T (p.Leu718=) rs145121387 0.00042
NM_001003699.4(RREB1):c.4578G>C (p.Thr1526=) rs148742062 0.00042
NM_001003699.4(RREB1):c.3177A>G (p.Thr1059=) rs368518533 0.00026
NM_001003699.4(RREB1):c.1020G>A (p.Ala340=) rs149913845 0.00024
NM_001003699.4(RREB1):c.1068C>T (p.Asp356=) rs139799223 0.00024
NM_001003699.4(RREB1):c.1263C>T (p.Gly421=) rs140980354 0.00024
NM_001003699.4(RREB1):c.480A>G (p.Pro160=) rs142510179 0.00016
NM_001003699.4(RREB1):c.1137C>T (p.Pro379=) rs376403896 0.00014
NM_001003699.4(RREB1):c.4920C>T (p.Ser1640=) rs141429177 0.00014
NM_001003699.4(RREB1):c.1389G>A (p.Ser463=) rs756737413 0.00013
NM_001003699.4(RREB1):c.1887G>A (p.Ala629=) rs111355837 0.00011
NM_001003699.4(RREB1):c.3168C>T (p.Pro1056=) rs137943791 0.00011
NM_001003699.4(RREB1):c.1710G>A (p.Gln570=) rs370148844 0.00010
NM_001003699.4(RREB1):c.2790C>T (p.Cys930=) rs764319083 0.00010
NM_001003699.4(RREB1):c.3585G>A (p.Pro1195=) rs772083408 0.00010
NM_001003699.4(RREB1):c.4170G>A (p.Pro1390=) rs143507762 0.00010
NM_001003699.4(RREB1):c.4589C>T (p.Ser1530Phe) rs116238548 0.00009
NM_001003699.4(RREB1):c.5034C>T (p.Ala1678=) rs368965053 0.00009
NM_001003699.4(RREB1):c.3114C>T (p.Gly1038=) rs563655407 0.00008
NM_001003699.4(RREB1):c.1038A>G (p.Glu346=) rs749360071 0.00006
NM_001003699.4(RREB1):c.2151C>T (p.His717=) rs147034062 0.00006
NM_001003699.4(RREB1):c.2793C>T (p.Ser931=) rs182302012 0.00006
NM_001003699.4(RREB1):c.4095T>C (p.Pro1365=) rs535277225 0.00006
NM_001003699.4(RREB1):c.2538G>A (p.Glu846=) rs531793725 0.00005
NM_001003699.4(RREB1):c.2619C>T (p.Gly873=) rs750916740 0.00005
NM_001003699.4(RREB1):c.5076G>A (p.Thr1692=) rs372269320 0.00005
NM_001003699.4(RREB1):c.898-6A>G rs774180539 0.00005
NM_001003699.4(RREB1):c.4734G>A (p.Ser1578=) rs1312760651 0.00004
NM_001003699.4(RREB1):c.4878C>T (p.His1626=) rs371285444 0.00004
NM_001003699.4(RREB1):c.1869C>T (p.Leu623=) rs764403342 0.00003
NM_001003699.4(RREB1):c.3366C>T (p.Ser1122=) rs369793962 0.00003
NM_001003699.4(RREB1):c.3540C>T (p.Ser1180=) rs1201405856 0.00003
NM_001003699.4(RREB1):c.765G>A (p.Ala255=) rs759101444 0.00003
NM_001003699.4(RREB1):c.1461G>A (p.Pro487=) rs753209205 0.00002
NM_001003699.4(RREB1):c.1905G>A (p.Thr635=) rs780891478 0.00002
NM_001003699.4(RREB1):c.2148G>T (p.Arg716=) rs544131983 0.00002
NM_001003699.4(RREB1):c.2352C>T (p.His784=) rs777078029 0.00002
NM_001003699.4(RREB1):c.4092G>T (p.Ala1364=) rs938143340 0.00002
NM_001003699.4(RREB1):c.693A>G (p.Ser231=) rs753643650 0.00002
NM_001003699.4(RREB1):c.831T>C (p.Ile277=) rs376195518 0.00002
NM_001003699.4(RREB1):c.2010A>G (p.Pro670=) rs769885102 0.00001
NM_001003699.4(RREB1):c.2139C>T (p.Asn713=) rs938426649 0.00001
NM_001003699.4(RREB1):c.2223G>T (p.Ala741=) rs375165183 0.00001
NM_001003699.4(RREB1):c.2550C>T (p.Cys850=) rs750223399 0.00001
NM_001003699.4(RREB1):c.2685C>T (p.Asp895=) rs748411454 0.00001
NM_001003699.4(RREB1):c.288C>T (p.Asp96=) rs893415056 0.00001
NM_001003699.4(RREB1):c.3165G>A (p.Lys1055=) rs781320502 0.00001
NM_001003699.4(RREB1):c.324G>A (p.Ser108=) rs56233031 0.00001
NM_001003699.4(RREB1):c.3981G>A (p.Gln1327=) rs1280398551 0.00001
NM_001003699.4(RREB1):c.414G>A (p.Gly138=) rs1367371356 0.00001
NM_001003699.4(RREB1):c.4587C>T (p.Pro1529=) rs1289283283 0.00001
NM_001003699.4(RREB1):c.4638T>C (p.Asp1546=) rs1581600760 0.00001
NM_001003699.4(RREB1):c.4735C>T (p.Leu1579=) rs747213067 0.00001
NM_001003699.4(RREB1):c.1057C>T (p.Leu353=) rs779786535
NM_001003699.4(RREB1):c.1287G>C (p.Ala429=) rs12192672
NM_001003699.4(RREB1):c.1554G>A (p.Val518=) rs1379976633
NM_001003699.4(RREB1):c.1726C>T (p.Arg576Trp) rs549745734
NM_001003699.4(RREB1):c.1731C>T (p.Leu577=) rs1338616765
NM_001003699.4(RREB1):c.2016G>A (p.Gln672=) rs572727664
NM_001003699.4(RREB1):c.2043C>T (p.Ala681=) rs1311213263
NM_001003699.4(RREB1):c.2115C>T (p.His705=) rs755410352
NM_001003699.4(RREB1):c.2310C>G (p.Ile770Met) rs555145261
NM_001003699.4(RREB1):c.2871G>A (p.Lys957=) rs1581575690
NM_001003699.4(RREB1):c.3195G>A (p.Leu1065=) rs1288957150
NM_001003699.4(RREB1):c.3609C>T (p.Asn1203=) rs149002354
NM_001003699.4(RREB1):c.4200T>C (p.Thr1400=) rs1366722570
NM_001003699.4(RREB1):c.4230G>C (p.Ala1410=) rs115475946
NM_001003699.4(RREB1):c.425+9G>A rs1581513375
NM_001003699.4(RREB1):c.4538_4555dup (p.Gly1513_Pro1518dup) rs745663065
NM_001003699.4(RREB1):c.4605G>T (p.Ala1535=) rs187170823
NM_001003699.4(RREB1):c.502T>C (p.Leu168=) rs1581542664

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