ClinVar Miner

List of variants in gene DAG1 reported as uncertain significance for cobblestone lissencephaly

Included ClinVar conditions (33):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 71
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HGVS dbSNP
NM_001165928.3(DAG1):c.1022C>T (p.Thr341Ile) rs148759919
NM_001165928.3(DAG1):c.1046C>T (p.Pro349Leu) rs200233956
NM_001165928.3(DAG1):c.1051A>G (p.Thr351Ala) rs376991799
NM_001165928.3(DAG1):c.1100C>T (p.Thr367Met)
NM_001165928.3(DAG1):c.1182C>T (p.Gly394=)
NM_001165928.3(DAG1):c.1186A>G (p.Thr396Ala) rs779846682
NM_001165928.3(DAG1):c.1210A>G (p.Thr404Ala) rs769229834
NM_001165928.3(DAG1):c.1215G>A (p.Met405Ile) rs141238609
NM_001165928.3(DAG1):c.1280C>T (p.Pro427Leu) rs770985285
NM_001165928.3(DAG1):c.1306A>G (p.Thr436Ala) rs149838438
NM_001165928.3(DAG1):c.1307C>T (p.Thr436Met) rs143573515
NM_001165928.3(DAG1):c.1360C>T (p.Arg454Trp) rs369872091
NM_001165928.3(DAG1):c.1369C>T (p.Arg457Trp)
NM_001165928.3(DAG1):c.1487G>T (p.Arg496Leu) rs199519832
NM_001165928.3(DAG1):c.1489C>G (p.Pro497Ala) rs376508721
NM_001165928.3(DAG1):c.148A>G (p.Met50Val) rs758104540
NM_001165928.3(DAG1):c.1492_1494del (p.Glu498del) rs1553653093
NM_001165928.3(DAG1):c.1535C>T (p.Thr512Ile) rs527867946
NM_001165928.3(DAG1):c.1543G>A (p.Glu515Lys)
NM_001165928.3(DAG1):c.1690C>A (p.Leu564Ile) rs199894361
NM_001165928.3(DAG1):c.1705C>T (p.His569Tyr) rs1559579950
NM_001165928.3(DAG1):c.1757C>T (p.Ser586Leu) rs371990100
NM_001165928.3(DAG1):c.1826A>G (p.Lys609Arg) rs200798800
NM_001165928.3(DAG1):c.1829C>T (p.Ala610Val)
NM_001165928.3(DAG1):c.1847C>T (p.Pro616Leu)
NM_001165928.3(DAG1):c.185C>T (p.Pro62Leu) rs375938350
NM_001165928.3(DAG1):c.1883_1887delinsACTTT (p.Ala628_Leu629delinsAspPhe) rs1559580384
NM_001165928.3(DAG1):c.193G>A (p.Val65Ile) rs757379579
NM_001165928.3(DAG1):c.1966G>A (p.Val656Met) rs1313375346
NM_001165928.3(DAG1):c.1977G>A (p.Trp659Ter) rs1553653437
NM_001165928.3(DAG1):c.2001G>T (p.Glu667Asp)
NM_001165928.3(DAG1):c.2023G>A (p.Ala675Thr)
NM_001165928.3(DAG1):c.2044G>A (p.Ala682Thr)
NM_001165928.3(DAG1):c.2100T>G (p.Phe700Leu) rs141697036
NM_001165928.3(DAG1):c.2123C>T (p.Thr708Met)
NM_001165928.3(DAG1):c.2124G>A (p.Thr708=)
NM_001165928.3(DAG1):c.212C>A (p.Thr71Lys)
NM_001165928.3(DAG1):c.2141G>A (p.Arg714Gln) rs201488118
NM_001165928.3(DAG1):c.2245G>A (p.Val749Ile) rs1559581311
NM_001165928.3(DAG1):c.2303G>T (p.Gly768Val) rs1553653701
NM_001165928.3(DAG1):c.2326C>T (p.Arg776Cys) rs752441031
NM_001165928.3(DAG1):c.2336G>A (p.Arg779Gln)
NM_001165928.3(DAG1):c.2342G>A (p.Gly781Asp)
NM_001165928.3(DAG1):c.2366C>T (p.Ala789Val) rs1426926145
NM_001165928.3(DAG1):c.23C>T (p.Ser8Leu)
NM_001165928.3(DAG1):c.2431C>T (p.Pro811Ser) rs368597067
NM_001165928.3(DAG1):c.244A>G (p.Ile82Val) rs141706514
NM_001165928.3(DAG1):c.2479C>T (p.Pro827Ser)
NM_001165928.3(DAG1):c.2512G>A (p.Glu838Lys)
NM_001165928.3(DAG1):c.2536A>C (p.Thr846Pro)
NM_001165928.3(DAG1):c.2552C>T (p.Thr851Met)
NM_001165928.3(DAG1):c.2561G>A (p.Arg854Gln) rs199933395
NM_001165928.3(DAG1):c.2576A>G (p.Asn859Ser) rs754079735
NM_001165928.3(DAG1):c.2588A>G (p.Tyr863Cys) rs1436774690
NM_001165928.3(DAG1):c.2635C>T (p.Arg879Cys)
NM_001165928.3(DAG1):c.268A>G (p.Ser90Gly) rs140454570
NM_001165928.3(DAG1):c.424G>A (p.Gly142Arg) rs749962207
NM_001165928.3(DAG1):c.496T>G (p.Ser166Ala) rs1421891404
NM_001165928.3(DAG1):c.576G>A (p.Thr192=)
NM_001165928.3(DAG1):c.613A>G (p.Lys205Glu) rs145871499
NM_001165928.3(DAG1):c.623T>C (p.Ile208Thr) rs772976299
NM_001165928.3(DAG1):c.634C>A (p.His212Asn) rs146574353
NM_001165928.3(DAG1):c.712A>G (p.Met238Val)
NM_001165928.3(DAG1):c.735G>A (p.Pro245=) rs748164001
NM_001165928.3(DAG1):c.751del (p.Val251fs)
NM_001165928.3(DAG1):c.829G>A (p.Val277Ile) rs375892170
NM_001165928.3(DAG1):c.854C>T (p.Ala285Val)
NM_001165928.3(DAG1):c.902A>G (p.Asn301Ser)
NM_001165928.3(DAG1):c.928G>A (p.Val310Ile)
NM_001165928.3(DAG1):c.932G>A (p.Arg311Gln) rs752813826
NM_001165928.3(DAG1):c.965C>T (p.Thr322Ile) rs376602004

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