ClinVar Miner

List of variants in gene DICER1 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_177438.3(DICER1):c.4891T>G (p.Ser1631Ala) rs145551486 0.00128
NM_177438.3(DICER1):c.4910C>T (p.Ser1637Leu) rs140875148 0.00108
NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr) rs149242330 0.00074
NM_177438.3(DICER1):c.3428T>C (p.Leu1143Pro) rs139786661 0.00070
NM_177438.3(DICER1):c.59C>T (p.Ala20Val) rs147660793 0.00070
NM_177438.3(DICER1):c.1233A>G (p.Ser411=) rs111595160 0.00057
NM_177438.3(DICER1):c.4206+11_4206+13del rs752585711 0.00043
NM_177438.3(DICER1):c.5337G>A (p.Lys1779=) rs111630745 0.00036
NM_177438.3(DICER1):c.3392A>G (p.Asn1131Ser) rs200651335 0.00030
NM_177438.3(DICER1):c.1124C>G (p.Pro375Arg) rs148758903 0.00025
NM_177438.3(DICER1):c.4773C>T (p.Leu1591=) rs138308365 0.00021
NM_177438.3(DICER1):c.4901T>C (p.Leu1634Ser) rs149723645 0.00021
NM_177438.3(DICER1):c.1839A>G (p.Pro613=) rs147754242 0.00018
NM_177438.3(DICER1):c.3261G>A (p.Ala1087=) rs369869162 0.00017
NM_177438.3(DICER1):c.4207-3C>T rs376041812 0.00017
NM_177438.3(DICER1):c.3553G>A (p.Ala1185Thr) rs150514959 0.00016
NM_177438.3(DICER1):c.4802A>T (p.Lys1601Met) rs181018393 0.00012
NM_177438.3(DICER1):c.5643T>C (p.Thr1881=) rs199574382 0.00012
NM_177438.3(DICER1):c.276T>C (p.Asn92=) rs370551656 0.00010
NM_177438.3(DICER1):c.439-7A>T rs376762569 0.00010
NM_177438.3(DICER1):c.5527+7T>A rs375239471 0.00009
NM_177438.3(DICER1):c.2337A>G (p.Thr779=) rs747210633 0.00008
NM_177438.3(DICER1):c.*5G>A rs770907156 0.00006
NM_177438.3(DICER1):c.1506A>G (p.Glu502=) rs754334322 0.00006
NM_177438.3(DICER1):c.3567T>C (p.Tyr1189=) rs141288912 0.00006
NM_177438.3(DICER1):c.3939G>A (p.Glu1313=) rs191567701 0.00006
NM_177438.3(DICER1):c.1827C>T (p.Asp609=) rs150087634 0.00005
NM_177438.3(DICER1):c.3741T>C (p.Ala1247=) rs765677895 0.00005
NM_177438.3(DICER1):c.4805C>G (p.Ala1602Gly) rs148955573 0.00005
NM_177438.3(DICER1):c.734+6C>T rs200212137 0.00005
NM_177438.3(DICER1):c.1329C>T (p.Cys443=) rs776143079 0.00004
NM_177438.3(DICER1):c.4101C>T (p.Ser1367=) rs370897400 0.00004
NM_177438.3(DICER1):c.4206+9_4206+23del rs766236360 0.00004
NM_177438.3(DICER1):c.4484C>T (p.Ser1495Leu) rs753527258 0.00004
NM_177438.3(DICER1):c.4554T>A (p.Val1518=) rs752773026 0.00004
NM_177438.3(DICER1):c.4896T>C (p.Ser1632=) rs376515225 0.00004
NM_177438.3(DICER1):c.5052C>G (p.Leu1684=) rs145027662 0.00004
NM_177438.3(DICER1):c.897G>A (p.Ser299=) rs201842071 0.00004
NM_177438.3(DICER1):c.1119A>C (p.Val373=) rs769274448 0.00003
NM_177438.3(DICER1):c.162A>C (p.Ala54=) rs776085363 0.00003
NM_177438.3(DICER1):c.2133T>C (p.His711=) rs878855248 0.00003
NM_177438.3(DICER1):c.574-19G>T rs372965421 0.00003
NM_177438.3(DICER1):c.1191C>T (p.Ser397=) rs780067844 0.00002
NM_177438.3(DICER1):c.1376+6T>C rs376417986 0.00002
NM_177438.3(DICER1):c.3210A>G (p.Leu1070=) rs547156371 0.00002
NM_177438.3(DICER1):c.3993A>G (p.Leu1331=) rs779318741 0.00002
NM_177438.3(DICER1):c.5625C>T (p.Asp1875=) rs781156066 0.00002
NM_177438.3(DICER1):c.909A>G (p.Leu303=) rs773509809 0.00002
NM_177438.3(DICER1):c.996C>T (p.Tyr332=) rs757094384 0.00002
NM_177438.3(DICER1):c.*4C>T rs774611849 0.00001
NM_177438.3(DICER1):c.126T>C (p.Tyr42=) rs774809100 0.00001
NM_177438.3(DICER1):c.1753-6G>A rs200569366 0.00001
NM_177438.3(DICER1):c.1758G>A (p.Leu586=) rs368558276 0.00001
NM_177438.3(DICER1):c.2229G>A (p.Thr743=) rs753276132 0.00001
NM_177438.3(DICER1):c.255C>G (p.Ile85Met) rs763422772 0.00001
NM_177438.3(DICER1):c.3465G>T (p.Thr1155=) rs377272036 0.00001
NM_177438.3(DICER1):c.3474C>T (p.Ser1158=) rs368984998 0.00001
NM_177438.3(DICER1):c.3987A>G (p.Thr1329=) rs373810197 0.00001
NM_177438.3(DICER1):c.4281G>A (p.Leu1427=) rs143985382 0.00001
NM_177438.3(DICER1):c.4509C>T (p.Tyr1503=) rs755994757 0.00001
NM_177438.3(DICER1):c.4698G>C (p.Leu1566=) rs372837448 0.00001
NM_177438.3(DICER1):c.5187G>A (p.Pro1729=) rs765113010 0.00001
NM_177438.3(DICER1):c.5190G>A (p.Gly1730=) rs371759757 0.00001
NM_177438.3(DICER1):c.5388A>G (p.Glu1796=) rs756025825 0.00001
NM_177438.3(DICER1):c.5748A>G (p.Gln1916=) rs763651908 0.00001
NM_177438.3(DICER1):c.129G>A (p.Thr43=) rs748819990
NM_177438.3(DICER1):c.1785T>C (p.Asp595=) rs1595406955
NM_177438.3(DICER1):c.18G>A (p.Leu6=) rs777350127
NM_177438.3(DICER1):c.1907+9T>C
NM_177438.3(DICER1):c.2313T>C (p.Tyr771=) rs1595382343
NM_177438.3(DICER1):c.2613C>T (p.Asp871=) rs759827733
NM_177438.3(DICER1):c.2754A>G (p.Thr918=) rs1595378905
NM_177438.3(DICER1):c.307+11del rs751519735
NM_177438.3(DICER1):c.354T>C (p.Asp118=) rs538838304
NM_177438.3(DICER1):c.3924T>C (p.Asp1308=)
NM_177438.3(DICER1):c.4050+12dup rs781354718
NM_177438.3(DICER1):c.4206+9_4206+29del
NM_177438.3(DICER1):c.5096-8C>T rs1566750853
NM_177438.3(DICER1):c.5391G>A (p.Glu1797=) rs751615662
NM_177438.3(DICER1):c.5527+7T>C rs375239471
NM_177438.3(DICER1):c.744T>A (p.Ser248=) rs1595448435

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.