List of variants in gene KCNT1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_020822.3(KCNT1):c.1612C>T (p.Arg538Cys)	rs774588571	0.00001
NM_020822.3(KCNT1):c.1061T>G (p.Met354Arg)	rs1057522923
NM_020822.3(KCNT1):c.1066C>T (p.Arg356Trp)	rs752514808
NM_020822.3(KCNT1):c.1226C>T (p.Pro409Leu)	rs1064794752
NM_020822.3(KCNT1):c.1309C>T (p.Leu437Phe)	rs1057518066
NM_020822.3(KCNT1):c.1420C>T (p.Arg474Cys)	rs866242631
NM_020822.3(KCNT1):c.1496A>G (p.His499Arg)	rs1554774362
NM_020822.3(KCNT1):c.2278A>T (p.Ile760Phe)	rs1064795013
NM_020822.3(KCNT1):c.2280C>G (p.Ile760Met)	rs370521183
NM_020822.3(KCNT1):c.2677G>A (p.Glu893Lys)	rs1554778082
NM_020822.3(KCNT1):c.2798G>A (p.Arg933His)	rs1023136319
NM_020822.3(KCNT1):c.2882G>A (p.Arg961His)	rs200694691
NM_020822.3(KCNT1):c.2944T>C (p.Ser982Pro)	rs1057523641
NM_020822.3(KCNT1):c.785G>A (p.Arg262Gln)	rs1554771469
NM_020822.3(KCNT1):c.841C>A (p.Leu281Ile)	rs1057522914

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