List of variants in gene DICER1 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_177438.3(DICER1):c.3972G>A (p.Lys1324=)	rs45562437	0.00174
NM_177438.3(DICER1):c.2115T>C (p.Ile705=)	rs140087741	0.00171
NM_177438.3(DICER1):c.20A>G (p.Gln7Arg)	rs117358479	0.00165
NM_177438.3(DICER1):c.*1506C>T	rs529235567	0.00132
NM_177438.3(DICER1):c.5145C>T (p.Leu1715=)	rs139500905	0.00121
NM_177438.3(DICER1):c.*997C>G	rs571363127	0.00097
NM_177438.3(DICER1):c.2614G>A (p.Ala872Thr)	rs149242330	0.00074
NM_177438.3(DICER1):c.59C>T (p.Ala20Val)	rs147660793	0.00070
NM_177438.3(DICER1):c.5203C>T (p.Leu1735=)	rs188609628	0.00059
NM_177438.3(DICER1):c.1124C>G (p.Pro375Arg)	rs148758903	0.00025
NM_177438.3(DICER1):c.3261G>A (p.Ala1087=)	rs369869162	0.00017
NM_177438.3(DICER1):c.3792G>A (p.Thr1264=)	rs778862635	0.00015
NM_177438.3(DICER1):c.5643T>C (p.Thr1881=)	rs199574382	0.00012
NM_177438.3(DICER1):c.2337A>G (p.Thr779=)	rs747210633	0.00008
NM_177438.3(DICER1):c.2720T>C (p.Ile907Thr)	rs200408568	0.00006
NM_177438.3(DICER1):c.1827C>T (p.Asp609=)	rs150087634	0.00005
NM_177438.3(DICER1):c.4554T>A (p.Val1518=)	rs752773026	0.00004
NM_177438.3(DICER1):c.897G>A (p.Ser299=)	rs201842071	0.00004
NM_177438.3(DICER1):c.3675C>T (p.Tyr1225=)	rs184830847	0.00003
NM_177438.3(DICER1):c.3993A>G (p.Leu1331=)	rs779318741	0.00002
NM_177438.3(DICER1):c.4638C>T (p.Tyr1546=)	rs773822569	0.00002
NM_177438.3(DICER1):c.747G>A (p.Gln249=)	rs376070315	0.00002
NM_177438.3(DICER1):c.1143C>T (p.Leu381=)	rs372592852	0.00001
NM_177438.3(DICER1):c.225A>G (p.Val75=)	rs750568225	0.00001
NM_177438.3(DICER1):c.2553G>A (p.Gln851=)	rs373715574	0.00001
NM_177438.3(DICER1):c.3315A>G (p.Lys1105=)	rs571852264	0.00001
NM_177438.3(DICER1):c.4509C>T (p.Tyr1503=)	rs755994757	0.00001
NM_177438.3(DICER1):c.5529A>G (p.Glu1843=)	rs768311617	0.00001
NM_177438.3(DICER1):c.846T>C (p.Asn282=)	rs1289583170	0.00001
NM_177438.3(DICER1):c.1510-4del	rs546524688
NM_177438.3(DICER1):c.2277T>C (p.Asp759=)
NM_177438.3(DICER1):c.2949C>T (p.Leu983=)	rs1555370277
NM_177438.3(DICER1):c.4206+7_4206+10del
NM_177438.3(DICER1):c.4254GGA[2] (p.Glu1420del)	rs544960260
NM_177438.3(DICER1):c.486T>G (p.Gly162=)
NM_177438.3(DICER1):c.5442G>T (p.Ser1814=)	rs759875628

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