ClinVar Miner

List of variants in gene AFF2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002025.4(AFF2):c.3088A>C (p.Ile1030Leu) rs149653283 0.00046
NM_002025.4(AFF2):c.1097A>G (p.His366Arg) rs199574795 0.00043
NM_002025.4(AFF2):c.2424C>T (p.Asp808=) rs139807832 0.00017
NM_002025.4(AFF2):c.1238C>T (p.Ser413Phe) rs782179754 0.00007
NM_002025.4(AFF2):c.896C>T (p.Pro299Leu) rs368459122 0.00006
NM_002025.4(AFF2):c.1541G>C (p.Arg514Pro) rs369100046 0.00005
NM_002025.4(AFF2):c.3270C>T (p.Phe1090=) rs371376716 0.00005
NM_002025.4(AFF2):c.1830G>C (p.Leu610Phe) rs200450195 0.00003
NM_002025.4(AFF2):c.3670G>A (p.Ala1224Thr) rs374197610 0.00003
NM_002025.4(AFF2):c.178T>C (p.Tyr60His) rs1298554052 0.00002
NM_002025.4(AFF2):c.2776C>T (p.Arg926Cys) rs1312069228 0.00002
NM_002025.4(AFF2):c.3100C>A (p.Leu1034Ile) rs782243009 0.00002
NM_002025.4(AFF2):c.3847C>T (p.Pro1283Ser) rs1326755554 0.00002
NM_002025.4(AFF2):c.481C>A (p.Arg161Ser) rs782411248 0.00002
NM_002025.4(AFF2):c.566C>T (p.Ser189Phe) rs782397628 0.00002
NM_002025.4(AFF2):c.1262+6T>C rs782244962 0.00001
NM_002025.4(AFF2):c.1460C>T (p.Ser487Phe) rs1057523435 0.00001
NM_002025.4(AFF2):c.1558C>A (p.Pro520Thr) rs899028170 0.00001
NM_002025.4(AFF2):c.181-6T>C rs797044705 0.00001
NM_002025.4(AFF2):c.1842G>T (p.Leu614Phe) rs371160275 0.00001
NM_002025.4(AFF2):c.2614G>C (p.Glu872Gln) rs2072067846 0.00001
NM_002025.4(AFF2):c.2903T>C (p.Ile968Thr) rs782123832 0.00001
NM_002025.4(AFF2):c.2913+7A>G rs1557288292 0.00001
NM_002025.4(AFF2):c.3038C>T (p.Thr1013Met) rs969709894 0.00001
NM_002025.4(AFF2):c.359A>G (p.Asn120Ser) rs1557257822 0.00001
NM_002025.4(AFF2):c.443T>G (p.Leu148Arg) rs912241826 0.00001
NM_002025.4(AFF2):c.64C>T (p.Arg22Cys) rs372514798 0.00001
NM_002025.4(AFF2):c.781C>T (p.Pro261Ser) rs886044832 0.00001
NM_002025.4(AFF2):c.926T>C (p.Ile309Thr) rs782518861 0.00001
GRCh37/hg19 Xq28(chrX:147625478-148258048)x3
GRCh37/hg19 Xq28(chrX:147775880-148546644)x3
GRCh37/hg19 Xq28(chrX:147836583-148128379)x3
GRCh37/hg19 Xq28(chrX:147891807-147993972)x2
NM_002025.4(AFF2):c.1016A>T (p.Lys339Met) rs2124469469
NM_002025.4(AFF2):c.1041+56413A>G
NM_002025.4(AFF2):c.1045A>G (p.Ser349Gly) rs2124640425
NM_002025.4(AFF2):c.1114C>T (p.Leu372Phe) rs1036551142
NM_002025.4(AFF2):c.1118C>G (p.Thr373Ser) rs587780276
NM_002025.4(AFF2):c.1123A>G (p.Met375Val)
NM_002025.4(AFF2):c.1129A>G (p.Thr377Ala) rs2070544297
NM_002025.4(AFF2):c.1173G>A (p.Gln391=) rs929635504
NM_002025.4(AFF2):c.1181A>G (p.Gln394Arg)
NM_002025.4(AFF2):c.1210+4A>G rs2124671930
NM_002025.4(AFF2):c.1228A>G (p.Thr410Ala)
NM_002025.4(AFF2):c.1256T>C (p.Phe419Ser)
NM_002025.4(AFF2):c.1262+1G>C rs782019909
NM_002025.4(AFF2):c.1262C>T (p.Ser421Leu)
NM_002025.4(AFF2):c.1285C>G (p.Leu429Val) rs782618037
NM_002025.4(AFF2):c.1309G>C (p.Glu437Gln)
NM_002025.4(AFF2):c.1424C>G (p.Pro475Arg) rs782601167
NM_002025.4(AFF2):c.142T>C (p.Phe48Leu)
NM_002025.4(AFF2):c.143T>A (p.Phe48Tyr)
NM_002025.4(AFF2):c.1444G>A (p.Gly482Arg)
NM_002025.4(AFF2):c.1467A>T (p.Glu489Asp) rs782268933
NM_002025.4(AFF2):c.1487C>T (p.Ser496Leu) rs2071997289
NM_002025.4(AFF2):c.148C>A (p.Leu50Ile) rs2054208339
NM_002025.4(AFF2):c.1511C>T (p.Thr504Ile)
NM_002025.4(AFF2):c.1541G>A (p.Arg514His) rs369100046
NM_002025.4(AFF2):c.1625A>G (p.Lys542Arg) rs1603348128
NM_002025.4(AFF2):c.164A>G (p.Tyr55Cys)
NM_002025.4(AFF2):c.1651A>G (p.Thr551Ala)
NM_002025.4(AFF2):c.1675C>A (p.Pro559Thr)
NM_002025.4(AFF2):c.1708A>G (p.Met570Val)
NM_002025.4(AFF2):c.1861G>A (p.Val621Met)
NM_002025.4(AFF2):c.1871G>A (p.Arg624Lys)
NM_002025.4(AFF2):c.189A>C (p.Lys63Asn)
NM_002025.4(AFF2):c.1942C>T (p.Pro648Ser)
NM_002025.4(AFF2):c.199C>T (p.Leu67Phe) rs1057521925
NM_002025.4(AFF2):c.2009G>A (p.Arg670His) rs1569557647
NM_002025.4(AFF2):c.2056C>T (p.Pro686Ser) rs868995963
NM_002025.4(AFF2):c.2082G>T (p.Lys694Asn) rs1603348350
NM_002025.4(AFF2):c.2086A>G (p.Lys696Glu) rs2124360234
NM_002025.4(AFF2):c.2113C>T (p.Pro705Ser)
NM_002025.4(AFF2):c.2171A>T (p.Gln724Leu)
NM_002025.4(AFF2):c.2219G>T (p.Gly740Val) rs2072037719
NM_002025.4(AFF2):c.2278A>T (p.Met760Leu)
NM_002025.4(AFF2):c.2296AAC[2] (p.Asn768del) rs782696162
NM_002025.4(AFF2):c.230A>T (p.Asn77Ile)
NM_002025.4(AFF2):c.243G>T (p.Met81Ile)
NM_002025.4(AFF2):c.2473A>G (p.Lys825Glu)
NM_002025.4(AFF2):c.2504C>G (p.Pro835Arg)
NM_002025.4(AFF2):c.251T>C (p.Leu84Ser)
NM_002025.4(AFF2):c.2533G>A (p.Glu845Lys)
NM_002025.4(AFF2):c.2568+5_2568+13del rs781810959
NM_002025.4(AFF2):c.256A>C (p.Thr86Pro) rs2124468283
NM_002025.4(AFF2):c.2588A>G (p.Lys863Arg)
NM_002025.4(AFF2):c.2668C>T (p.His890Tyr)
NM_002025.4(AFF2):c.2693A>G (p.Asn898Ser)
NM_002025.4(AFF2):c.26A>G (p.Asp9Gly)
NM_002025.4(AFF2):c.2921A>T (p.Asp974Val)
NM_002025.4(AFF2):c.2929A>G (p.Lys977Glu)
NM_002025.4(AFF2):c.2950A>G (p.Ile984Val)
NM_002025.4(AFF2):c.297G>C (p.Lys99Asn)
NM_002025.4(AFF2):c.3046A>C (p.Thr1016Pro) rs2124386181
NM_002025.4(AFF2):c.3079A>G (p.Thr1027Ala)
NM_002025.4(AFF2):c.3085A>G (p.Thr1029Ala)
NM_002025.4(AFF2):c.3167C>T (p.Thr1056Ile)
NM_002025.4(AFF2):c.31G>A (p.Asp11Asn)
NM_002025.4(AFF2):c.3220T>C (p.Tyr1074His)
NM_002025.4(AFF2):c.3267+5G>C rs374064624
NM_002025.4(AFF2):c.3298G>A (p.Ala1100Thr)
NM_002025.4(AFF2):c.3305C>T (p.Ala1102Val)
NM_002025.4(AFF2):c.3313T>C (p.Ser1105Pro)
NM_002025.4(AFF2):c.3374C>T (p.Thr1125Ile)
NM_002025.4(AFF2):c.3395A>G (p.Glu1132Gly) rs2124402692
NM_002025.4(AFF2):c.3405-1G>T rs1557290471
NM_002025.4(AFF2):c.340T>C (p.Phe114Leu) rs1057523628
NM_002025.4(AFF2):c.3427T>G (p.Phe1143Val)
NM_002025.4(AFF2):c.3431C>A (p.Ala1144Glu)
NM_002025.4(AFF2):c.3477-4A>G
NM_002025.4(AFF2):c.3482G>A (p.Arg1161Gln) rs2124413129
NM_002025.4(AFF2):c.3497T>C (p.Leu1166Pro)
NM_002025.4(AFF2):c.3576T>C (p.Asn1192=) rs797044666
NM_002025.4(AFF2):c.3606A>G (p.Pro1202=) rs886044827
NM_002025.4(AFF2):c.3631C>T (p.Pro1211Ser)
NM_002025.4(AFF2):c.3697G>A (p.Val1233Ile) rs1557291713
NM_002025.4(AFF2):c.3739G>A (p.Val1247Ile)
NM_002025.4(AFF2):c.3776A>T (p.His1259Leu)
NM_002025.4(AFF2):c.3814+1G>T
NM_002025.4(AFF2):c.3815-5T>C rs2072529658
NM_002025.4(AFF2):c.3827A>G (p.Asp1276Gly) rs1569558083
NM_002025.4(AFF2):c.3872C>T (p.Thr1291Ile)
NM_002025.4(AFF2):c.407T>A (p.Met136Lys) rs782692812
NM_002025.4(AFF2):c.410C>T (p.Pro137Leu)
NM_002025.4(AFF2):c.449A>G (p.His150Arg)
NM_002025.4(AFF2):c.495C>A (p.Asn165Lys) rs797044704
NM_002025.4(AFF2):c.511G>C (p.Ala171Pro)
NM_002025.4(AFF2):c.659G>T (p.Ser220Ile)
NM_002025.4(AFF2):c.670T>A (p.Ser224Thr)
NM_002025.4(AFF2):c.791G>T (p.Gly264Val)
NM_002025.4(AFF2):c.803A>G (p.Gln268Arg) rs2054318590
NM_002025.4(AFF2):c.811C>T (p.Pro271Ser)
NM_002025.4(AFF2):c.898G>T (p.Asp300Tyr)
NM_002025.4(AFF2):c.95G>A (p.Arg32Gln) rs782129403
NM_002025.4(AFF2):c.982C>G (p.Pro328Ala)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.