ClinVar Miner

List of variants reported as benign for Benign Neonatal Epilepsy by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_004519.4(KCNQ3):c.*1050A>C rs76720699
NM_004519.4(KCNQ3):c.*1407A>C rs76570743
NM_004519.4(KCNQ3):c.*1754C>T rs977939
NM_004519.4(KCNQ3):c.*2137C>T rs2272679
NM_004519.4(KCNQ3):c.*2475C>T rs141143602
NM_004519.4(KCNQ3):c.*3032A>G rs2469626
NM_004519.4(KCNQ3):c.*3035A>G rs2469627
NM_004519.4(KCNQ3):c.*3597G>A rs1025436
NM_004519.4(KCNQ3):c.*396A>G rs78243592
NM_004519.4(KCNQ3):c.*3977G>A rs2469628
NM_004519.4(KCNQ3):c.*4125T>C rs2163608
NM_004519.4(KCNQ3):c.*4243A>T rs2436131
NM_004519.4(KCNQ3):c.*425C>A rs10956641
NM_004519.4(KCNQ3):c.*426C>G rs10956640
NM_004519.4(KCNQ3):c.*4746_*4747insACAG rs112550767
NM_004519.4(KCNQ3):c.*4958A>G rs1437824
NM_004519.4(KCNQ3):c.*4982A>T rs545252668
NM_004519.4(KCNQ3):c.*4982del rs35772668
NM_004519.4(KCNQ3):c.*5719C>T rs11786417
NM_004519.4(KCNQ3):c.*5932A>C rs2436130
NM_004519.4(KCNQ3):c.*6238T>C rs10108362
NM_004519.4(KCNQ3):c.*6282A>T rs10095295
NM_004519.4(KCNQ3):c.*6340G>A rs2469629
NM_004519.4(KCNQ3):c.*6632T>C rs9297840
NM_004519.4(KCNQ3):c.*6812A>G rs7815106
NM_004519.4(KCNQ3):c.*6874C>G rs2436129
NM_004519.4(KCNQ3):c.*6956A>G rs2469630
NM_004519.4(KCNQ3):c.*7033T>C rs2436128
NM_004519.4(KCNQ3):c.*7075A>G rs2436127
NM_004519.4(KCNQ3):c.*7095T>G rs1437823
NM_004519.4(KCNQ3):c.*7119C>T rs2436126
NM_004519.4(KCNQ3):c.*7131G>A rs75865310
NM_004519.4(KCNQ3):c.*7143A>G rs2436125
NM_004519.4(KCNQ3):c.*7221C>T rs2436124
NM_004519.4(KCNQ3):c.*7371T>G rs76268875
NM_004519.4(KCNQ3):c.*7506C>T rs11785257
NM_004519.4(KCNQ3):c.*8148G>A rs1437822
NM_004519.4(KCNQ3):c.-142G>T rs28606540
NM_004519.4(KCNQ3):c.1071C>G (p.Leu357=) rs17575754
NM_004519.4(KCNQ3):c.1241A>G (p.Glu414Gly) rs2303995
NM_004519.4(KCNQ3):c.660T>C (p.Asn220=) rs41272389
NM_004519.4(KCNQ3):c.732T>C (p.Gly244=) rs41272387

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