ClinVar Miner

List of variants in gene DNM1 reported as benign for Lennox-Gastaut syndrome

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_004408.4(DNM1):c.1196+4C>T
NM_004408.4(DNM1):c.1197-7C>T rs41306488
NM_004408.4(DNM1):c.1423-8C>A rs555786484
NM_004408.4(DNM1):c.1437C>T (p.Ile479=) rs141788807
NM_004408.4(DNM1):c.1493+14del rs371426966
NM_004408.4(DNM1):c.1558-3C>T rs546517702
NM_004408.4(DNM1):c.1662G>A (p.Lys554=)
NM_004408.4(DNM1):c.1764C>T (p.Leu588=) rs111534551
NM_004408.4(DNM1):c.1782-9A>G rs201739236
NM_004408.4(DNM1):c.1889T>C (p.Val630Ala)
NM_004408.4(DNM1):c.1906-6T>C rs138961089
NM_004408.4(DNM1):c.1933G>A (p.Asp645Asn)
NM_004408.4(DNM1):c.2156C>G (p.Ala719Gly)
NM_004408.4(DNM1):c.2318+10C>T
NM_004408.4(DNM1):c.2360C>T (p.Ala787Val) rs1363606775
NM_004408.4(DNM1):c.2420C>G (p.Ser807Cys) rs935756107
NM_004408.4(DNM1):c.2540C>T (p.Ser847Leu) rs199498658
NM_004408.4(DNM1):c.2541G>A (p.Ser847=) rs545142847
NM_004408.4(DNM1):c.332C>G (p.Thr111Ser) rs192913494
NM_004408.4(DNM1):c.357T>C (p.Pro119=) rs77325628
NM_004408.4(DNM1):c.450C>G (p.Pro150=) rs143834670
NM_004408.4(DNM1):c.747C>T (p.Thr249=) rs141651183
NM_004408.4(DNM1):c.825C>G (p.Pro275=)

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