ClinVar Miner

List of variants in gene KCNT1 reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

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Total variants: 24
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HGVS dbSNP
NM_020822.3(KCNT1):c.1036-7C>T rs774394132
NM_020822.3(KCNT1):c.1173C>T (p.Asn391=) rs374015551
NM_020822.3(KCNT1):c.1326C>A (p.Leu442=) rs200910140
NM_020822.3(KCNT1):c.1566C>T (p.Ile522=)
NM_020822.3(KCNT1):c.1718G>A (p.Arg573His) rs575162600
NM_020822.3(KCNT1):c.1746C>T (p.Tyr582=) rs763438119
NM_020822.3(KCNT1):c.1769+8C>T rs371287985
NM_020822.3(KCNT1):c.1854C>T (p.Ala618=)
NM_020822.3(KCNT1):c.1899G>A (p.Ser633=) rs371135108
NM_020822.3(KCNT1):c.1962C>T (p.His654=) rs141759469
NM_020822.3(KCNT1):c.2052G>A (p.Thr684=) rs376314779
NM_020822.3(KCNT1):c.2412C>T (p.Ile804=) rs559452456
NM_020822.3(KCNT1):c.2729G>A (p.Arg910Gln) rs151272083
NM_020822.3(KCNT1):c.273C>T (p.Tyr91=) rs770619151
NM_020822.3(KCNT1):c.2895C>T (p.Ala965=) rs776550763
NM_020822.3(KCNT1):c.3001A>G (p.Thr1001Ala) rs143780942
NM_020822.3(KCNT1):c.3012G>A (p.Ser1004=) rs751965012
NM_020822.3(KCNT1):c.3042G>A (p.Glu1014=)
NM_020822.3(KCNT1):c.3156+8G>A rs764262230
NM_020822.3(KCNT1):c.3495C>T (p.Thr1165=) rs374429090
NM_020822.3(KCNT1):c.3588C>T (p.Val1196=)
NM_020822.3(KCNT1):c.3618C>T (p.His1206=) rs577378740
NM_020822.3(KCNT1):c.477C>G (p.Ser159=) rs200157100
NM_020822.3(KCNT1):c.99A>G (p.Gln33=) rs146152956

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