ClinVar Miner

List of variants reported as benign for Lennox-Gastaut syndrome by Invitae

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_001271.4(CHD2):c.1017G>A (p.Glu339=) rs141957556
NM_001271.4(CHD2):c.1170A>G (p.Lys390=) rs1342167975
NM_001271.4(CHD2):c.153C>T (p.Ser51=) rs201752698
NM_001271.4(CHD2):c.1788T>C (p.Tyr596=) rs144093014
NM_001271.4(CHD2):c.1995G>A (p.Pro665=) rs747900073
NM_001271.4(CHD2):c.2337A>G (p.Gly779=) rs138084718
NM_001271.4(CHD2):c.2353-10A>G rs190159225
NM_001271.4(CHD2):c.2577+7T>C rs146944583
NM_001271.4(CHD2):c.2728-3C>T rs2272460
NM_001271.4(CHD2):c.2730A>T (p.Val910=) rs77895180
NM_001271.4(CHD2):c.3126C>T (p.Asp1042=) rs150268140
NM_001271.4(CHD2):c.3279G>A (p.Arg1093=) rs774908145
NM_001271.4(CHD2):c.330G>A (p.Arg110=) rs138626801
NM_001271.4(CHD2):c.3315G>A (p.Thr1105=) rs138979360
NM_001271.4(CHD2):c.3321C>T (p.Asp1107=) rs141018126
NM_001271.4(CHD2):c.3400G>A (p.Ala1134Thr) rs147466101
NM_001271.4(CHD2):c.3540C>T (p.Ser1180=) rs76621355
NM_001271.4(CHD2):c.3573G>A (p.Gln1191=) rs79219767
NM_001271.4(CHD2):c.4058C>T (p.Pro1353Leu) rs755088564
NM_001271.4(CHD2):c.4061G>A (p.Arg1354Lys) rs370160870
NM_001271.4(CHD2):c.4138-6T>C rs182330071
NM_001271.4(CHD2):c.4219T>A (p.Ser1407Thr) rs61756301
NM_001271.4(CHD2):c.4284A>G (p.Lys1428=) rs35339954
NM_001271.4(CHD2):c.4518G>A (p.Leu1506=) rs557766333
NM_001271.4(CHD2):c.4527C>T (p.Ile1509=) rs34315566
NM_001271.4(CHD2):c.4721G>C (p.Gly1574Ala) rs56227200
NM_001271.4(CHD2):c.4724G>C (p.Gly1575Ala)
NM_001271.4(CHD2):c.4807C>T (p.Pro1603Ser) rs144395162
NM_001271.4(CHD2):c.4874A>G (p.Asn1625Ser) rs143431217
NM_001271.4(CHD2):c.4901A>C (p.Asn1634Thr)
NM_001271.4(CHD2):c.5047G>A (p.Ala1683Thr) rs747794466
NM_001271.4(CHD2):c.5049C>T (p.Ala1683=) rs139534358
NM_001271.4(CHD2):c.5050C>T (p.His1684Tyr) rs746849506
NM_001271.4(CHD2):c.5104C>G (p.Gln1702Glu)
NM_001271.4(CHD2):c.5106G>A (p.Gln1702=) rs781108294
NM_001271.4(CHD2):c.516A>G (p.Gln172=) rs770631510
NM_001271.4(CHD2):c.5268G>C (p.Gln1756His) rs201950393
NM_001271.4(CHD2):c.608A>G (p.Lys203Arg) rs117844037
NM_001271.4(CHD2):c.826+4T>C rs369930157
NM_001271.4(CHD2):c.854C>T (p.Ala285Val) rs544867753
NM_001271.4(CHD2):c.855G>A (p.Ala285=) rs138796857
NM_001271.4(CHD2):c.907G>A (p.Gly303Ser) rs200687736
NM_001271.4(CHD2):c.960A>T (p.Thr320=) rs149632554
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=) rs371589347
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.46C>A (p.Leu16Met) rs61757224
NM_004408.4(DNM1):c.6C>T (p.Gly2=)
NM_004408.4(DNM1):c.747C>T (p.Thr249=) rs141651183
NM_004408.4(DNM1):c.825C>G (p.Pro275=) rs1588357060

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