ClinVar Miner

List of variants in gene DPM3 studied for Congenital disorder of glycosylation type 1O

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Total variants: 20
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HGVS dbSNP
NC_000001.11:g.(?_155139952)_(155140340_?)dup
NM_153741.2(DPM3):c.124C>G (p.Pro42Ala) rs745692004
NM_153741.2(DPM3):c.127G>A (p.Ala43Thr)
NM_153741.2(DPM3):c.176A>C (p.Tyr59Ser) rs1055439022
NM_153741.2(DPM3):c.178C>T (p.Arg60Cys)
NM_153741.2(DPM3):c.179G>T (p.Arg60Leu) rs773427971
NM_153741.2(DPM3):c.185C>T (p.Ala62Val) rs1553190791
NM_153741.2(DPM3):c.208G>A (p.Ala70Thr)
NM_153741.2(DPM3):c.218A>C (p.Glu73Ala) rs745807155
NM_153741.2(DPM3):c.21G>A (p.Trp7Ter) rs1444066075
NM_153741.2(DPM3):c.249C>A (p.Ala83=) rs193215070
NM_153741.2(DPM3):c.254T>A (p.Leu85Ter) rs121908155
NM_153741.2(DPM3):c.254T>C (p.Leu85Ser) rs121908155
NM_153741.2(DPM3):c.266G>A (p.Gly89Glu)
NM_153741.2(DPM3):c.28G>C (p.Gly10Arg)
NM_153741.2(DPM3):c.41T>C (p.Leu14Pro) rs778481307
NM_153741.2(DPM3):c.48C>T (p.Ser16=) rs753265590
NM_153741.2(DPM3):c.55G>T (p.Val19Leu) rs141877691
NM_153741.2(DPM3):c.60C>T (p.Ala20=) rs371295542
NM_153741.2(DPM3):c.95T>C (p.Leu32Ser) rs959102245

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