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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 45

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.1029dup (p.Phe344fs)	rs1555374772
NM_177438.3(DICER1):c.1174C>T (p.Arg392Ter)	rs1131691211
NM_177438.3(DICER1):c.1355dup (p.Tyr452Ter)	rs1595438021
NM_177438.3(DICER1):c.1836del (p.Pro613fs)	rs1595406359
NM_177438.3(DICER1):c.1907+1G>A	rs1131691217
NM_177438.3(DICER1):c.1908-1G>T	rs1595397289
NM_177438.3(DICER1):c.2281dup (p.Tyr761fs)	rs1595382528
NM_177438.3(DICER1):c.2379T>G (p.Tyr793Ter)	rs1595382041
NM_177438.3(DICER1):c.238G>T (p.Glu80Ter)	rs1595466234
NM_177438.3(DICER1):c.2436+1G>T	rs1595381795
NM_177438.3(DICER1):c.2551C>T (p.Gln851Ter)
NM_177438.3(DICER1):c.2606_2607del (p.Pro869fs)	rs1595380210
NM_177438.3(DICER1):c.2628C>A (p.Tyr876Ter)	rs1406824963
NM_177438.3(DICER1):c.2642T>C (p.Leu881Pro)	rs1595380007
NM_177438.3(DICER1):c.2651-1G>C	rs1595379448
NM_177438.3(DICER1):c.2767A>T (p.Lys923Ter)	rs1357513890
NM_177438.3(DICER1):c.3071G>A (p.Trp1024Ter)	rs751053813
NM_177438.3(DICER1):c.3269+1G>A	rs1595370466
NM_177438.3(DICER1):c.3293G>A (p.Trp1098Ter)	rs1595367992
NM_177438.3(DICER1):c.3665dup (p.Leu1222fs)	rs1595365532
NM_177438.3(DICER1):c.3675C>A (p.Tyr1225Ter)	rs184830847
NM_177438.3(DICER1):c.3737del (p.Asn1246fs)	rs1595365114
NM_177438.3(DICER1):c.3957dup (p.Asp1320fs)	rs1566766788
NM_177438.3(DICER1):c.3988del (p.Tyr1330fs)	rs1595363945
NM_177438.3(DICER1):c.4005C>A (p.Tyr1335Ter)	rs755357184
NM_177438.3(DICER1):c.4050+1G>A	rs875989783
NM_177438.3(DICER1):c.4051-1G>A	rs1595354013
NM_177438.3(DICER1):c.4140G>A (p.Trp1380Ter)	rs1131691205
NM_177438.3(DICER1):c.4206+1G>T	rs765059994
NM_177438.3(DICER1):c.438+1G>A	rs1595462667
NM_177438.3(DICER1):c.4405_4406del (p.Leu1469fs)	rs1064795904
NM_177438.3(DICER1):c.4442G>A (p.Trp1481Ter)	rs1595341418
NM_177438.3(DICER1):c.4458dup (p.Ser1487fs)	rs1131691197
NM_177438.3(DICER1):c.4633dup (p.Ser1545fs)	rs875989781
NM_177438.3(DICER1):c.4654C>T (p.Gln1552Ter)	rs1131691208
NM_177438.3(DICER1):c.4956_4959del (p.His1652fs)	rs1595338209
NM_177438.3(DICER1):c.5013_5017del (p.Lys1671fs)	rs1595337717
NM_177438.3(DICER1):c.5095+1G>A	rs886037722
NM_177438.3(DICER1):c.5103C>A (p.Tyr1701Ter)	rs875989780
NM_177438.3(DICER1):c.5138A>T (p.Asp1713Val)	rs1595331224
NM_177438.3(DICER1):c.5389_5392del (p.Glu1797fs)	rs1595315137
NM_177438.3(DICER1):c.5479del (p.Leu1827fs)	rs1555366197
NM_177438.3(DICER1):c.714_717del (p.Asp239fs)	rs1595456687
NM_177438.3(DICER1):c.727_730del (p.Leu243fs)	rs1595456594
NM_177438.3(DICER1):c.809_812dup (p.Met272fs)	rs1595448006

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.