List of variants in gene DNMT1 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.*165T>G	rs192952800	0.00132
NM_001130823.3(DNMT1):c.*253G>A	rs768761819	0.00038
NM_001130823.3(DNMT1):c.2667C>T (p.Tyr889=)	rs199832007	0.00013
NM_001130823.3(DNMT1):c.*274T>C	rs886054125	0.00009
NM_001130823.3(DNMT1):c.483T>C (p.Thr161=)	rs764496230	0.00009
NM_001130823.3(DNMT1):c.*29G>A	rs749247799	0.00008
NM_001130823.3(DNMT1):c.*211G>C	rs772999851	0.00006
NM_001130823.3(DNMT1):c.*126A>G	rs886054126	0.00003
NM_001130823.3(DNMT1):c.-26C>T	rs745759875	0.00003
NM_001130823.3(DNMT1):c.3117-4G>A	rs781402268	0.00003
NM_001130823.3(DNMT1):c.886G>A (p.Glu296Lys)	rs891770194	0.00003
NM_001130823.3(DNMT1):c.867C>T (p.Asp289=)	rs750916721	0.00002
NM_001130823.3(DNMT1):c.2807G>A (p.Arg936Gln)	rs763321599	0.00001
NM_001130823.3(DNMT1):c.3117-8G>A	rs769623856	0.00001
NM_001130823.3(DNMT1):c.3343C>T (p.Pro1115Ser)	rs755865204	0.00001
NM_001130823.3(DNMT1):c.3394+7C>T	rs886054128	0.00001
NM_001130823.3(DNMT1):c.3537G>A (p.Thr1179=)	rs761140414	0.00001
NM_001130823.3(DNMT1):c.3567G>A (p.Ala1189=)	rs746163207	0.00001
NM_001130823.3(DNMT1):c.4074C>T (p.Ser1358=)	rs2089536795	0.00001
NM_001130823.3(DNMT1):c.4164C>T (p.Ser1388=)	rs779701784	0.00001
NM_001130823.3(DNMT1):c.4204A>T (p.Ile1402Phe)	rs886054127	0.00001
NM_001130823.3(DNMT1):c.500C>G (p.Pro167Arg)	rs886054129	0.00001
NM_001130823.3(DNMT1):c.526A>C (p.Lys176Gln)	rs1020363356	0.00001
NM_001130823.3(DNMT1):c.720A>G (p.Arg240=)	rs760733624	0.00001
NM_001130823.3(DNMT1):c.916C>T (p.Pro306Ser)	rs761747950	0.00001
NM_001130823.3(DNMT1):c.*18C>T	rs778467461
NM_001130823.3(DNMT1):c.*34A>C	rs1416080045
NM_001130823.3(DNMT1):c.-34C>G	rs112908248
NM_001130823.3(DNMT1):c.1044-18dup	rs59599980
NM_001130823.3(DNMT1):c.1171-7C>T	rs1168540279
NM_001130823.3(DNMT1):c.1191G>A (p.Leu397=)	rs1599371468
NM_001130823.3(DNMT1):c.2100G>A (p.Gln700=)	rs2038347997
NM_001130823.3(DNMT1):c.3294C>G (p.Arg1098=)	rs775786809
NM_001130823.3(DNMT1):c.3580C>T (p.Arg1194Trp)	rs1255153711

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