ClinVar Miner

List of variants in gene DPM2 reported as likely benign for congenital disorder of glycosylation type I

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_003863.3(DPM2):c.-382C>T rs112813338 0.01257
NM_003863.4(DPM2):c.183G>A (p.Leu61=) rs11552794 0.01027
NM_003863.4(DPM2):c.177C>T (p.Leu59=) rs35334863 0.00922
NM_003863.4(DPM2):c.64A>G (p.Thr22Ala) rs7042788 0.00120
NM_003863.4(DPM2):c.102C>T (p.Ile34=) rs777078287 0.00006
NM_003863.4(DPM2):c.3+14C>A rs375782774 0.00006
NM_003863.4(DPM2):c.197-5C>T rs886063482 0.00005
NM_003863.4(DPM2):c.39C>G (p.Leu13=) rs757467123 0.00004
NM_003863.4(DPM2):c.94-19G>A rs760505582 0.00004
NM_003863.4(DPM2):c.94-9C>T rs373340697 0.00004
NM_003863.4(DPM2):c.114T>C (p.His38=) rs1482824230 0.00001
NM_003863.4(DPM2):c.144C>T (p.Ala48=) rs779110103 0.00001
NM_003863.4(DPM2):c.33C>T (p.Leu11=) rs781596486 0.00001
NM_003863.4(DPM2):c.93+13C>A rs772691262 0.00001
NM_003863.4(DPM2):c.94-8G>T rs773731630 0.00001
NM_003863.4(DPM2):c.120C>T (p.Ile40=) rs1588689780
NM_003863.4(DPM2):c.153C>A (p.Val51=)
NM_003863.4(DPM2):c.178C>T (p.Leu60=) rs2131648105
NM_003863.4(DPM2):c.180G>A (p.Leu60=) rs2131648100
NM_003863.4(DPM2):c.196+12C>T
NM_003863.4(DPM2):c.196+13C>T
NM_003863.4(DPM2):c.196+18C>G
NM_003863.4(DPM2):c.196+19C>T rs769003503
NM_003863.4(DPM2):c.196+20C>T
NM_003863.4(DPM2):c.237G>A (p.Val79=)
NM_003863.4(DPM2):c.27G>C (p.Val9=)
NM_003863.4(DPM2):c.3+12A>T
NM_003863.4(DPM2):c.3+14C>T
NM_003863.4(DPM2):c.3+15G>T
NM_003863.4(DPM2):c.3+16T>C
NM_003863.4(DPM2):c.39C>T (p.Leu13=) rs757467123
NM_003863.4(DPM2):c.4-18G>C
NM_003863.4(DPM2):c.66C>A (p.Thr22=) rs532790675
NM_003863.4(DPM2):c.66C>G (p.Thr22=) rs532790675
NM_003863.4(DPM2):c.93+14C>T rs1831525625
NM_003863.4(DPM2):c.93+17G>A
NM_003863.4(DPM2):c.93+17G>C
NM_003863.4(DPM2):c.94-11C>T
NM_003863.4(DPM2):c.94-14del rs760202275
NM_003863.4(DPM2):c.94-18C>G rs577196007
NM_003863.4(DPM2):c.94-19G>C
NM_003863.4(DPM2):c.94-19G>T
NM_003863.4(DPM2):c.94-4C>T rs1588689814

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