List of variants in gene DNMT1 reported as uncertain significance 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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.520A>C (p.Thr174Pro)	rs201319352	0.00009
NM_001130823.3(DNMT1):c.3223C>T (p.Arg1075Cys)	rs140852137	0.00006
NM_001130823.3(DNMT1):c.3519A>C (p.Gln1173His)	rs151305495	0.00002
NM_001130823.3(DNMT1):c.3595G>A (p.Gly1199Ser)	rs780717834	0.00002
NM_001130823.3(DNMT1):c.3437C>G (p.Pro1146Arg)	rs1412256768	0.00001
NM_001130823.3(DNMT1):c.4445G>A (p.Arg1482His)	rs770535972	0.00001
NM_001130823.3(DNMT1):c.1191G>A (p.Leu397=)	rs1599371468
NM_001130823.3(DNMT1):c.1303C>G (p.Leu435Val)	rs1555691714
NM_001130823.3(DNMT1):c.2433C>G (p.His811Gln)	rs1599359716
NM_001130823.3(DNMT1):c.2721-8T>C
NM_001130823.3(DNMT1):c.2894+4A>G
NM_001130823.3(DNMT1):c.3140C>T (p.Thr1047Ile)
NM_001130823.3(DNMT1):c.3832T>C (p.Phe1278Leu)	rs535946725
NM_001130823.3(DNMT1):c.4091A>G (p.Lys1364Arg)	rs1369475967
NM_001130823.3(DNMT1):c.410C>T (p.Thr137Met)	rs377146699
NM_001130823.3(DNMT1):c.4372A>G (p.Ile1458Val)	rs1599341541
NM_001130823.3(DNMT1):c.4414C>T (p.Arg1472Trp)	rs2089501636
NM_001130823.3(DNMT1):c.804-8T>C

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