ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 105
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001048174.2(MUTYH):c.115+151G>A rs3219486 0.03415
NM_001048174.2(MUTYH):c.1517G>A (p.Arg506Gln) rs3219497 0.01092
NM_001048174.2(MUTYH):c.-7+1625C>T rs3219473 0.01083
NM_001048174.2(MUTYH):c.1460C>T (p.Ser487Phe) rs140118273 0.00997
NM_001048174.2(MUTYH):c.-7+401C>T rs3219470 0.00686
NM_001048174.2(MUTYH):c.1347G>C (p.Thr449=) rs74318065 0.00596
NM_001048174.2(MUTYH):c.116-338A>G rs146659156 0.00510
NM_001048174.2(MUTYH):c.-7+1616G>A rs115736558 0.00426
NM_001048174.2(MUTYH):c.1392+228C>T rs3219491 0.00373
NM_001048174.2(MUTYH):c.1103-27C>T rs3219490 0.00300
NM_001048174.2(MUTYH):c.304+56G>A rs201858839 0.00274
NM_001048174.2(MUTYH):c.1501C>A (p.Leu501Met) rs3219496 0.00154
NM_001048174.2(MUTYH):c.1192C>T (p.Arg398Cys) rs150792276 0.00081
NM_001048174.2(MUTYH):c.841C>T (p.Arg281Cys) rs138089183 0.00051
NM_001048174.2(MUTYH):c.914-9C>T rs3219488 0.00045
NM_001048174.2(MUTYH):c.11C>T (p.Pro4Leu) rs79777494 0.00044
NM_001048174.2(MUTYH):c.32G>A (p.Gly11Asp) rs75321043 0.00044
NM_001048174.2(MUTYH):c.1365C>T (p.Thr455=) rs150269172 0.00043
NM_001048174.2(MUTYH):c.1174C>A (p.Leu392Met) rs144079536 0.00041
NM_001048174.2(MUTYH):c.850-2A>G rs77542170 0.00035
NM_001048174.2(MUTYH):c.1102+17C>T rs369034810 0.00020
NM_001048174.2(MUTYH):c.1102+9A>T rs587780742 0.00018
NM_001128425.2(MUTYH):c.42C>T (p.Ile14=) rs202240122 0.00017
NM_001048174.2(MUTYH):c.1393-17C>G rs199664013 0.00012
NM_001048174.2(MUTYH):c.1034C>T (p.Ala345Val) rs35352891 0.00011
NM_001048174.2(MUTYH):c.132G>A (p.Pro44=) rs144551668 0.00011
NM_001048174.2(MUTYH):c.1464G>A (p.Pro488=) rs143796254 0.00011
NM_001048174.2(MUTYH):c.-6-7G>A rs780029247 0.00010
NM_001048174.2(MUTYH):c.606+14C>G rs752537118 0.00009
NM_001048174.2(MUTYH):c.612C>T (p.Thr204=) rs780747266 0.00009
NM_001048174.2(MUTYH):c.1400G>A (p.Arg467His) rs144111588 0.00008
NM_001048174.2(MUTYH):c.929A>G (p.Gln310Arg) rs199742231 0.00008
NM_001048174.2(MUTYH):c.1107G>T (p.Leu369=) rs201412035 0.00007
NM_001048174.2(MUTYH):c.21C>T (p.Ala7=) rs201982344 0.00007
NM_001048174.2(MUTYH):c.492+8G>C rs190500741 0.00007
NM_001048174.2(MUTYH):c.305-13C>G rs201207780 0.00006
NM_001048174.2(MUTYH):c.729C>T (p.Asp243=) rs730881838 0.00006
NM_001048174.2(MUTYH):c.897T>C (p.Pro299=) rs149334084 0.00006
NM_001048174.2(MUTYH):c.630C>T (p.Asn210=) rs767327888 0.00005
NM_001048174.2(MUTYH):c.99G>A (p.Lys33=) rs375084663 0.00005
NM_001048174.2(MUTYH):c.1062C>T (p.Ala354=) rs778193554 0.00004
NM_001048174.2(MUTYH):c.1446G>A (p.Arg482=) rs747201171 0.00004
NM_001048174.2(MUTYH):c.305-6C>T rs376600220 0.00004
NM_001048174.2(MUTYH):c.325C>T (p.Leu109=) rs368963039 0.00004
NM_001048174.2(MUTYH):c.564G>A (p.Gly188=) rs760562341 0.00004
NM_001048174.2(MUTYH):c.704+9T>C rs143091801 0.00004
NM_001048174.2(MUTYH):c.797G>A (p.Arg266His) rs146044717 0.00004
NM_001048174.2(MUTYH):c.87C>T (p.Asn29=) rs141679570 0.00004
NM_001048174.2(MUTYH):c.366C>T (p.Thr122=) rs368383907 0.00003
NM_001048174.2(MUTYH):c.900C>T (p.Asp300=) rs587780752 0.00003
NM_001048174.2(MUTYH):c.1131G>A (p.Pro377=) rs876659935 0.00002
NM_001048174.2(MUTYH):c.183C>T (p.Asp61=) rs538419476 0.00002
NM_001048174.2(MUTYH):c.1134C>T (p.Ser378=) rs759460243 0.00001
NM_001048174.2(MUTYH):c.1155G>A (p.Glu385=) rs754860019 0.00001
NM_001048174.2(MUTYH):c.116-75C>T rs1481053395 0.00001
NM_001048174.2(MUTYH):c.1194T>C (p.Arg398=) rs777361121 0.00001
NM_001048174.2(MUTYH):c.1206C>T (p.Pro402=) rs752408891 0.00001
NM_001048174.2(MUTYH):c.1218G>A (p.Thr406=) rs751465584 0.00001
NM_001048174.2(MUTYH):c.1311A>C (p.Pro437=) rs768239149 0.00001
NM_001048174.2(MUTYH):c.1320C>T (p.Thr440=) rs746668146 0.00001
NM_001048174.2(MUTYH):c.1380C>T (p.Thr460=) rs373973053 0.00001
NM_001048174.2(MUTYH):c.138G>A (p.Glu46=) rs376861118 0.00001
NM_001048174.2(MUTYH):c.216G>A (p.Leu72=) rs766958451 0.00001
NM_001048174.2(MUTYH):c.288C>T (p.Asp96=) rs730881836 0.00001
NM_001048174.2(MUTYH):c.36C>T (p.His12=) rs776396492 0.00001
NM_001048174.2(MUTYH):c.378+3G>A rs373939052 0.00001
NM_001048174.2(MUTYH):c.507A>C (p.Leu169=) rs754061478 0.00001
NM_001048174.2(MUTYH):c.573A>C (p.Thr191=) rs778014929 0.00001
NM_001048174.2(MUTYH):c.594C>T (p.Ile198=) rs371875647 0.00001
NM_001048174.2(MUTYH):c.704+7T>A rs369052315 0.00001
NM_001048174.2(MUTYH):c.705-20G>T rs1645059942 0.00001
NM_001048174.2(MUTYH):c.78T>A (p.Ala26=) rs199968813 0.00001
NM_001048174.2(MUTYH):c.798C>T (p.Arg266=) rs587780750 0.00001
NM_001048174.2(MUTYH):c.802C>T (p.Leu268=) rs778782508 0.00001
NM_001048174.2(MUTYH):c.867C>G (p.Leu289=) rs11211096 0.00001
NM_001048174.2(MUTYH):c.870A>G (p.Leu290=) rs1553127406 0.00001
NM_001048174.2(MUTYH):c.903G>C (p.Val301=) rs749048388 0.00001
NM_001048174.2(MUTYH):c.96C>A (p.Ala32=) rs778968451 0.00001
NM_001048174.2(MUTYH):c.*34GTT[1] rs373507005
NM_001048174.2(MUTYH):c.1116A>G (p.Gly372=) rs1570377075
NM_001048174.2(MUTYH):c.1137G>C (p.Val379=) rs1553125948
NM_001048174.2(MUTYH):c.1209C>G (p.Leu403=) rs577542506
NM_001048174.2(MUTYH):c.1236G>C (p.Gly412=) rs1553125459
NM_001048174.2(MUTYH):c.1347G>A (p.Thr449=) rs74318065
NM_001048174.2(MUTYH):c.1363A>C (p.Thr455Pro) rs1570363119
NM_001048174.2(MUTYH):c.1393-9_1393-7del rs763940868
NM_001048174.2(MUTYH):c.1413C>T (p.Gly471=)
NM_001048174.2(MUTYH):c.1435-7T>C rs1396143193
NM_001048174.2(MUTYH):c.1509T>C (p.Asn503=) rs876659054
NM_001048174.2(MUTYH):c.172C>T (p.Leu58=) rs781163298
NM_001048174.2(MUTYH):c.228C>T (p.Tyr76=) rs121908380
NM_001048174.2(MUTYH):c.305-4C>A rs767717597
NM_001048174.2(MUTYH):c.390A>T (p.Thr130=) rs780182847
NM_001048174.2(MUTYH):c.546G>A (p.Gln182=) rs1553128516
NM_001048174.2(MUTYH):c.606+21C>A rs148552450
NM_001048174.2(MUTYH):c.607-11C>T rs1057522026
NM_001048174.2(MUTYH):c.645G>A (p.Leu215=) rs1060504204
NM_001048174.2(MUTYH):c.663T>C (p.Ile221=) rs577792676
NM_001048174.2(MUTYH):c.771A>G (p.Leu257=) rs876658503
NM_001048174.2(MUTYH):c.774G>A (p.Gly258=) rs771290019
NM_001048174.2(MUTYH):c.888G>A (p.Ser296=) rs771683103
NM_001048174.2(MUTYH):c.924T>C (p.Thr308=) rs924192790
NM_001048174.2(MUTYH):c.929_930delinsGC (p.Gln310Arg) rs587780083
NM_001048174.2(MUTYH):c.943C>T (p.Leu315=) rs1455263014
NM_001128425.2(MUTYH):c.167G>T (p.Gly56Val) rs587781374

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.