List of variants in gene DNMT1 reported as uncertain significance for cerebellar disorder

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.2315C>A (p.Thr772Asn)	rs142562681	0.00010
NM_001130823.3(DNMT1):c.*211G>C	rs772999851	0.00006
NM_001130823.3(DNMT1):c.4483G>A (p.Val1495Met)	rs781301028	0.00006
NM_001130823.3(DNMT1):c.695C>T (p.Pro232Leu)	rs758190156	0.00006
NM_001130823.3(DNMT1):c.3157G>A (p.Ala1053Thr)	rs370786558	0.00004
NM_001130823.3(DNMT1):c.855C>T (p.Gly285=)	rs755151805	0.00003
NM_001130823.3(DNMT1):c.857T>C (p.Val286Ala)	rs766504703	0.00003
NM_001130823.3(DNMT1):c.3167A>G (p.Asn1056Ser)	rs767308840	0.00002
NM_001130823.3(DNMT1):c.3353A>G (p.His1118Arg)	rs150331990	0.00002
NM_001130823.3(DNMT1):c.3394+4C>T	rs781376510	0.00002
NM_001130823.3(DNMT1):c.3498G>T (p.Gly1166=)	rs1186008456	0.00002
NM_001130823.3(DNMT1):c.1008G>A (p.Lys336=)	rs750048459	0.00001
NM_001130823.3(DNMT1):c.4001C>T (p.Ala1334Val)	rs766051225	0.00001
NM_001130823.3(DNMT1):c.898A>C (p.Lys300Gln)	rs759143980	0.00001
NM_001130823.3(DNMT1):c.937C>T (p.Arg313Trp)	rs1372902099	0.00001
NM_001130823.3(DNMT1):c.2718C>G (p.Phe906Leu)	rs1057518774
NM_001130823.3(DNMT1):c.2920C>T (p.Arg974Cys)	rs2089651800
NM_001130823.3(DNMT1):c.3042G>C (p.Glu1014Asp)	rs745780816
NM_001130823.3(DNMT1):c.3311C>T (p.Ala1104Val)	rs2089593597
NM_001130823.3(DNMT1):c.382C>T (p.Pro128Ser)	rs146601335
NM_001130823.3(DNMT1):c.4136G>A (p.Arg1379Gln)	rs2145258691
NM_001130823.3(DNMT1):c.650A>G (p.Asp217Gly)	rs1568249130
NM_001130823.3(DNMT1):c.859C>G (p.Gln287Glu)	rs2145340495
NM_001130823.3(DNMT1):c.910A>C (p.Ser304Arg)	rs1599376406

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