ClinVar Miner

List of variants in gene DAG1 reported as likely benign for cobblestone lissencephaly

Included ClinVar conditions (33):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_001165928.3(DAG1):c.1014C>T (p.Ile338=) rs773685771
NM_001165928.3(DAG1):c.1026C>T (p.Pro342=) rs1553652858
NM_001165928.3(DAG1):c.1122C>T (p.Gly374=) rs139993618
NM_001165928.3(DAG1):c.1308G>A (p.Thr436=) rs143763229
NM_001165928.3(DAG1):c.1401C>T (p.Ser467=) rs1222765845
NM_001165928.3(DAG1):c.1773C>T (p.Phe591=) rs2229010
NM_001165928.3(DAG1):c.2036G>A (p.Arg679His) rs113904914
NM_001165928.3(DAG1):c.2082C>T (p.Asn694=) rs146453412
NM_001165928.3(DAG1):c.2313C>T (p.Ala771=) rs764289801
NM_001165928.3(DAG1):c.24G>A (p.Ser8=) rs1229832209
NM_001165928.3(DAG1):c.2511C>T (p.Pro837=) rs778665335
NM_001165928.3(DAG1):c.258G>C (p.Leu86Phe) rs145403829
NM_001165928.3(DAG1):c.278T>C (p.Ile93Thr) rs149218670
NM_001165928.3(DAG1):c.286-10del rs747305463
NM_001165928.3(DAG1):c.384G>A (p.Val128=) rs143829263
NM_001165928.3(DAG1):c.402C>T (p.Ser134=) rs367603470
NM_001165928.3(DAG1):c.57C>T (p.Leu19=) rs768105958
NM_001165928.3(DAG1):c.591C>T (p.Ala197=) rs768487898
NM_001165928.3(DAG1):c.599C>G (p.Thr200Ser) rs41290704

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