ClinVar Miner

List of variants in gene TCOF1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_001371623.1(TCOF1):c.2340+294G>C rs2569061 0.98525
NM_001371623.1(TCOF1):c.640-223G>A rs2255796 0.39611
NM_001371623.1(TCOF1):c.4172C>T (p.Ala1391Val) rs15251 0.21165
NM_001371623.1(TCOF1):c.2660T>C (p.Val887Ala) rs7713638 0.18279
NM_001371623.1(TCOF1):c.1842A>G (p.Ser614=) rs2071239 0.18176
NM_001371623.1(TCOF1):c.1578C>T (p.Pro526=) rs2071238 0.17747
NM_001371623.1(TCOF1):c.2859+4010A>G rs7715100 0.17735
NM_001371623.1(TCOF1):c.304+161C>T rs891941 0.16651
NM_001371623.1(TCOF1):c.3530C>G (p.Pro1177Arg) rs1136103 0.15799
NM_001371623.1(TCOF1):c.1761G>T (p.Gly587=) rs7701163 0.09554
NM_001371623.1(TCOF1):c.3183+102G>C rs56287670 0.09361
NM_001371623.1(TCOF1):c.3518-31G>A rs78716239 0.09269
NM_001371623.1(TCOF1):c.3604-3C>T rs11743855 0.08821
NM_001371623.1(TCOF1):c.4346-139C>T rs11167501 0.08509
NM_001371623.1(TCOF1):c.3297+66C>T rs11742769 0.08118
NC_000005.10:g.150357401C>T rs28372960 0.06146
NM_001371623.1(TCOF1):c.304+202C>T rs7703914 0.06053
NM_001371623.1(TCOF1):c.2859+169G>A rs148432105 0.05562
NM_001371623.1(TCOF1):c.639+244C>T rs78451313 0.05541
NM_001371623.1(TCOF1):c.639+32C>T rs77741284 0.05450
NM_001371623.1(TCOF1):c.1083+39G>A rs56113366 0.05067
NM_001371623.1(TCOF1):c.1489-82G>A rs73270845 0.03948
NM_001371623.1(TCOF1):c.4345+223A>C rs191495968 0.02677
NM_001371623.1(TCOF1):c.4346-193A>G rs142671991 0.02256
NM_001371623.1(TCOF1):c.3183+68A>G rs115488540 0.02201
NM_001371623.1(TCOF1):c.2859+3703G>A rs114416816 0.02161
NM_001371623.1(TCOF1):c.4295G>C (p.Gly1432Ala) rs45491898 0.01804
NM_001371623.1(TCOF1):c.2859+3967G>T rs11950303 0.01775
NM_001371623.1(TCOF1):c.2859+49G>A rs7732047 0.01546
NM_001371623.1(TCOF1):c.1229C>T (p.Ser410Leu) rs114326915 0.01242
NM_001371623.1(TCOF1):c.4053G>A (p.Ser1351=) rs114169102 0.01206
NM_001371623.1(TCOF1):c.162A>G (p.Gln54=) rs73270831 0.01015
NM_001371623.1(TCOF1):c.2245C>T (p.Pro749Ser) rs73270846 0.00993
NM_001371623.1(TCOF1):c.4007A>G (p.Lys1336Arg) rs55980697 0.00865
NM_001371623.1(TCOF1):c.1783G>A (p.Val595Ile) rs75583421 0.00814
NM_001371623.1(TCOF1):c.3510C>T (p.His1170=) rs116354094 0.00617
NM_001371623.1(TCOF1):c.579G>A (p.Ala193=) rs142965998 0.00558
NM_001371623.1(TCOF1):c.2762C>T (p.Pro921Leu) rs150515843 0.00548
NM_001371623.1(TCOF1):c.1281G>A (p.Ala427=) rs113299143 0.00291
NM_001371623.1(TCOF1):c.3594G>A (p.Ala1198=) rs148626720 0.00272
NM_001371623.1(TCOF1):c.109-13T>C rs147327313 0.00267
NM_001371623.1(TCOF1):c.295G>A (p.Ala99Thr) rs112332762 0.00260
NM_001371623.1(TCOF1):c.122C>T (p.Ala41Val) rs56180593 0.00232
NM_001371623.1(TCOF1):c.3712G>A (p.Ala1238Thr) rs137960641 0.00205
NM_001371623.1(TCOF1):c.3426C>T (p.Ser1142=) rs138291748 0.00197
NM_001371623.1(TCOF1):c.2859+3389G>T rs151344575 0.00196
NM_001371623.1(TCOF1):c.1269G>A (p.Ala423=) rs72492454 0.00193
NM_001371623.1(TCOF1):c.1028G>A (p.Ser343Asn) rs144327167 0.00188
NM_001371623.1(TCOF1):c.2088T>G (p.Ser696Arg) rs140334121 0.00149
NM_001371623.1(TCOF1):c.1671T>C (p.Asp557=) rs142758482 0.00135
NM_001371623.1(TCOF1):c.2151T>A (p.Ser717=) rs141764046 0.00135
NM_001371623.1(TCOF1):c.534C>T (p.Ser178=) rs141250614 0.00132
NM_001371623.1(TCOF1):c.1300C>T (p.Pro434Ser) rs143519179 0.00129
NM_001371623.1(TCOF1):c.3623T>A (p.Met1208Lys) rs139081024 0.00114
NM_001371623.1(TCOF1):c.3168G>A (p.Glu1056=) rs78239421 0.00111
NM_001371623.1(TCOF1):c.999G>A (p.Gly333=) rs55918703 0.00104
NM_001371623.1(TCOF1):c.1034A>G (p.Glu345Gly) rs150637771 0.00102
NM_001371623.1(TCOF1):c.3339G>A (p.Gln1113=) rs147074393 0.00086
NM_001371623.1(TCOF1):c.1120G>T (p.Ala374Ser) rs112039991 0.00079
NM_001371623.1(TCOF1):c.1723A>G (p.Ile575Val) rs35918007 0.00074
NM_001371623.1(TCOF1):c.1535T>C (p.Met512Thr) rs201458471 0.00072
NM_001371623.1(TCOF1):c.1590G>A (p.Gly530=) rs145539529 0.00071
NM_001371623.1(TCOF1):c.3538A>T (p.Thr1180Ser) rs144793475 0.00053
NM_001371623.1(TCOF1):c.1390G>A (p.Ala464Thr) rs150956690 0.00051
NM_001371623.1(TCOF1):c.1502G>A (p.Gly501Glu) rs201581867 0.00048
NM_001371623.1(TCOF1):c.4248C>T (p.Asp1416=) rs141159244 0.00042
NM_001371623.1(TCOF1):c.2731G>T (p.Ala911Ser) rs557426457 0.00041
NM_001371623.1(TCOF1):c.2842G>T (p.Ala948Ser) rs181102251 0.00036
NM_001371623.1(TCOF1):c.3241G>A (p.Ala1081Thr) rs112144548 0.00033
NM_001371623.1(TCOF1):c.2000G>A (p.Arg667Gln) rs146735293 0.00032
NM_001371623.1(TCOF1):c.866G>A (p.Ser289Asn) rs188279654 0.00029
NM_001371623.1(TCOF1):c.1547C>T (p.Pro516Leu) rs138645438 0.00028
NM_001371623.1(TCOF1):c.2332C>T (p.Pro778Ser) rs368225177 0.00026
NM_001371623.1(TCOF1):c.4418C>T (p.Pro1473Leu) rs148367422 0.00026
NM_001371623.1(TCOF1):c.3191A>G (p.Lys1064Arg) rs149117118 0.00025
NM_001371623.1(TCOF1):c.961G>A (p.Gly321Arg) rs146307766 0.00024
NM_001371623.1(TCOF1):c.3493G>C (p.Gly1165Arg) rs141095369 0.00018
NM_001371623.1(TCOF1):c.3335C>T (p.Pro1112Leu) rs140440910 0.00014
NM_001371623.1(TCOF1):c.4284G>T (p.Thr1428=) rs148889187 0.00013
NM_001371623.1(TCOF1):c.3537G>A (p.Arg1179=) rs200202637 0.00010
NM_001371623.1(TCOF1):c.1714T>C (p.Leu572=) rs111705180 0.00009
NM_001371623.1(TCOF1):c.4388A>G (p.Lys1463Arg) rs200645401 0.00008
NM_001371623.1(TCOF1):c.1854G>A (p.Ala618=) rs151344570 0.00006
NM_001371623.1(TCOF1):c.4182C>T (p.Asp1394=) rs200273817 0.00006
NM_001371623.1(TCOF1):c.3628C>T (p.Pro1210Ser) rs558530968 0.00005
NM_001371623.1(TCOF1):c.630A>G (p.Thr210=) rs765654624 0.00005
NM_001371623.1(TCOF1):c.4023G>A (p.Lys1341=) rs199890846 0.00002
NM_001371623.1(TCOF1):c.1867G>A (p.Ala623Thr) rs201126288 0.00001
NM_001371623.1(TCOF1):c.3518-3C>T rs543072968 0.00001
NM_001371623.1(TCOF1):c.1993G>C (p.Ala665Pro) rs2071240
NM_001371623.1(TCOF1):c.2395G>T (p.Ala799Ser) rs373946807
NM_001371623.1(TCOF1):c.4326GAA[2] (p.Lys1445del) rs574569798
NM_001371623.1(TCOF1):c.4374GAA[2] (p.Lys1461del) rs151344581
NM_001371623.1(TCOF1):c.4444-132C>A rs11744415
NM_001371623.1(TCOF1):c.4444-221G>C rs2569062
NM_001371623.1(TCOF1):c.827_844del (p.Gly276_Glu281del) rs528897827

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