ClinVar Miner

List of variants in gene RAI1 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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Total variants: 99
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HGVS dbSNP gnomAD frequency
NM_030665.4(RAI1):c.3589G>C (p.Gly1197Arg) rs200719553 0.00024
NM_030665.4(RAI1):c.2981G>A (p.Arg994Gln) rs201996411 0.00016
NM_030665.4(RAI1):c.1273A>G (p.Asn425Asp) rs142539314 0.00015
NM_030665.4(RAI1):c.1580G>A (p.Arg527His) rs377314203 0.00011
NM_030665.4(RAI1):c.1925C>T (p.Ser642Leu) rs200061071 0.00009
NM_030665.4(RAI1):c.3883C>T (p.Pro1295Ser) rs372337877 0.00009
NM_030665.4(RAI1):c.3158C>T (p.Pro1053Leu) rs748386061 0.00007
NM_030665.4(RAI1):c.2951C>T (p.Ala984Val) rs371644042 0.00006
NM_030665.4(RAI1):c.3895G>A (p.Asp1299Asn) rs750911924 0.00006
NM_030665.4(RAI1):c.397C>T (p.Pro133Ser) rs183251531 0.00006
NM_030665.4(RAI1):c.5528T>C (p.Phe1843Ser) rs145732429 0.00006
NM_030665.4(RAI1):c.5717C>T (p.Pro1906Leu) rs754508586 0.00006
NM_030665.4(RAI1):c.757G>A (p.Ala253Thr) rs758931451 0.00006
NM_030665.4(RAI1):c.125G>A (p.Arg42Gln) rs200367247 0.00005
NM_030665.4(RAI1):c.2225A>G (p.Asn742Ser) rs527512369 0.00005
NM_030665.4(RAI1):c.4726C>T (p.Arg1576Cys) rs199790171 0.00005
NM_030665.4(RAI1):c.1979G>A (p.Arg660Gln) rs377537260 0.00004
NM_030665.4(RAI1):c.3142G>T (p.Ala1048Ser) rs889706395 0.00004
NM_030665.4(RAI1):c.3479G>A (p.Arg1160Gln) rs764373875 0.00004
NM_030665.4(RAI1):c.3761A>G (p.Asn1254Ser) rs141204901 0.00004
NM_030665.4(RAI1):c.3884C>T (p.Pro1295Leu) rs376809177 0.00004
NM_030665.4(RAI1):c.4258T>C (p.Ser1420Pro) rs1446366935 0.00004
NM_030665.4(RAI1):c.719C>T (p.Thr240Ile) rs142646842 0.00004
NM_030665.4(RAI1):c.386C>G (p.Pro129Arg) rs748915017 0.00003
NM_030665.4(RAI1):c.4166A>G (p.Gln1389Arg) rs757354656 0.00003
NM_030665.4(RAI1):c.4355G>A (p.Arg1452Gln) rs368003493 0.00003
NM_030665.4(RAI1):c.73T>A (p.Ser25Thr) rs891764320 0.00003
NM_030665.4(RAI1):c.2414C>T (p.Ser805Leu) rs368058215 0.00002
NM_030665.4(RAI1):c.2545G>A (p.Asp849Asn) rs866732668 0.00002
NM_030665.4(RAI1):c.3097C>G (p.Pro1033Ala) rs749315193 0.00002
NM_030665.4(RAI1):c.4183G>C (p.Gly1395Arg) rs1458340042 0.00002
NM_030665.4(RAI1):c.4625G>A (p.Arg1542Gln) rs184604492 0.00002
NM_030665.4(RAI1):c.1202C>T (p.Thr401Met) rs200825036 0.00001
NM_030665.4(RAI1):c.1487C>T (p.Pro496Leu) rs200903510 0.00001
NM_030665.4(RAI1):c.2692A>G (p.Ile898Val) rs200306885 0.00001
NM_030665.4(RAI1):c.4816G>A (p.Ala1606Thr) rs575260371 0.00001
NM_030665.4(RAI1):c.5141A>G (p.Lys1714Arg) rs369948107 0.00001
NM_030665.4(RAI1):c.5170C>T (p.Arg1724Trp) rs373198856 0.00001
NM_030665.4(RAI1):c.530C>T (p.Pro177Leu) rs753632651 0.00001
NM_030665.4(RAI1):c.5432C>G (p.Ala1811Gly) rs1484029703 0.00001
NM_030665.4(RAI1):c.5702A>G (p.Lys1901Arg) rs779284444 0.00001
NM_030665.4(RAI1):c.688G>A (p.Gly230Arg) rs546550691 0.00001
NM_030665.4(RAI1):c.1030C>T (p.His344Tyr)
NM_030665.4(RAI1):c.1054C>T (p.Arg352Cys) rs907728820
NM_030665.4(RAI1):c.1063T>C (p.Ser355Pro)
NM_030665.4(RAI1):c.1098C>G (p.Asn366Lys)
NM_030665.4(RAI1):c.1424A>G (p.Gln475Arg)
NM_030665.4(RAI1):c.1579C>T (p.Arg527Cys)
NM_030665.4(RAI1):c.1603G>A (p.Ala535Thr) rs754428934
NM_030665.4(RAI1):c.1606C>T (p.Arg536Cys) rs149164900
NM_030665.4(RAI1):c.194C>T (p.Thr65Met)
NM_030665.4(RAI1):c.1970C>T (p.Ala657Val)
NM_030665.4(RAI1):c.199T>C (p.Ser67Pro) rs2143001498
NM_030665.4(RAI1):c.2029G>A (p.Gly677Ser) rs754646763
NM_030665.4(RAI1):c.2221G>A (p.Ala741Thr)
NM_030665.4(RAI1):c.2289C>T (p.Gly763=)
NM_030665.4(RAI1):c.2404_2406del (p.Lys802del) rs779691871
NM_030665.4(RAI1):c.2708A>G (p.Glu903Gly)
NM_030665.4(RAI1):c.2731A>C (p.Lys911Gln)
NM_030665.4(RAI1):c.3106G>A (p.Gly1036Arg)
NM_030665.4(RAI1):c.3254G>A (p.Gly1085Glu) rs756454905
NM_030665.4(RAI1):c.3346C>T (p.Pro1116Ser) rs950397097
NM_030665.4(RAI1):c.3407C>T (p.Thr1136Met)
NM_030665.4(RAI1):c.3440G>A (p.Arg1147Gln)
NM_030665.4(RAI1):c.3515G>A (p.Arg1172His)
NM_030665.4(RAI1):c.3553G>A (p.Ala1185Thr)
NM_030665.4(RAI1):c.3701C>T (p.Thr1234Ile)
NM_030665.4(RAI1):c.3724C>T (p.Arg1242Trp)
NM_030665.4(RAI1):c.3725G>A (p.Arg1242Gln)
NM_030665.4(RAI1):c.3730C>T (p.Arg1244Cys)
NM_030665.4(RAI1):c.3731GCA[5] (p.Ser1249del)
NM_030665.4(RAI1):c.3731GCA[7] (p.Ser1249dup) rs760919336
NM_030665.4(RAI1):c.3751G>A (p.Ala1251Thr)
NM_030665.4(RAI1):c.3754A>G (p.Ser1252Gly)
NM_030665.4(RAI1):c.3805C>T (p.Leu1269Phe)
NM_030665.4(RAI1):c.3920G>A (p.Arg1307Gln) rs369260099
NM_030665.4(RAI1):c.4129G>A (p.Gly1377Arg) rs767828696
NM_030665.4(RAI1):c.4228G>A (p.Gly1410Ser)
NM_030665.4(RAI1):c.4313G>C (p.Gly1438Ala) rs781252626
NM_030665.4(RAI1):c.4384C>G (p.Pro1462Ala)
NM_030665.4(RAI1):c.4436A>G (p.Asp1479Gly)
NM_030665.4(RAI1):c.4463G>T (p.Ser1488Ile)
NM_030665.4(RAI1):c.4523C>T (p.Ser1508Phe)
NM_030665.4(RAI1):c.4637A>G (p.Lys1546Arg)
NM_030665.4(RAI1):c.4905_4910del (p.Ser1638_Ser1639del)
NM_030665.4(RAI1):c.4927G>C (p.Asp1643His)
NM_030665.4(RAI1):c.5288C>A (p.Pro1763Gln)
NM_030665.4(RAI1):c.5365C>T (p.Arg1789Trp)
NM_030665.4(RAI1):c.5407C>T (p.Arg1803Cys) rs778987232
NM_030665.4(RAI1):c.5443C>G (p.Pro1815Ala)
NM_030665.4(RAI1):c.5470G>A (p.Val1824Met)
NM_030665.4(RAI1):c.5503G>A (p.Val1835Ile)
NM_030665.4(RAI1):c.5709G>A (p.Lys1903=)
NM_030665.4(RAI1):c.76C>T (p.Arg26Cys) rs376964045
NM_030665.4(RAI1):c.834GCA[20] (p.Gln285_Gln291dup) rs371983878
NM_030665.4(RAI1):c.834GCA[5] (p.Gln284_Gln291del) rs371983878
NM_030665.4(RAI1):c.836_837insACAGCA (p.Gln290_Gln291dup) rs587780428
NM_030665.4(RAI1):c.918A>T (p.Gln306His)
NM_030665.4(RAI1):c.986G>A (p.Arg329Gln)

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