List of variants in gene HCN1 reported as pathogenic for central nervous system disorder

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_021072.4(HCN1):c.1138A>T (p.Ile380Phe)	rs2112040738
NM_021072.4(HCN1):c.1159G>T (p.Ala387Ser)	rs2112040690
NM_021072.4(HCN1):c.1160C>G (p.Ala387Gly)
NM_021072.4(HCN1):c.1169T>C (p.Val390Ala)	rs2112040676
NM_021072.4(HCN1):c.1171G>A (p.Gly391Ser)	rs1561139569
NM_021072.4(HCN1):c.1172G>A (p.Gly391Asp)	rs1057519547
NM_021072.4(HCN1):c.1172G>T (p.Gly391Val)	rs1057519547
NM_021072.4(HCN1):c.1184C>G (p.Ala395Gly)	rs2112040633
NM_021072.4(HCN1):c.1201G>C (p.Asp401His)	rs587777491
NM_021072.4(HCN1):c.1240G>A (p.Val414Met)	rs1561120793
NM_021072.4(HCN1):c.1522G>A (p.Val508Met)	rs180790607
NM_021072.4(HCN1):c.1562G>T (p.Gly521Val)	rs1745671912
NM_021072.4(HCN1):c.1769G>A (p.Arg590Gln)	rs1561081319
NM_021072.4(HCN1):c.299C>T (p.Ser100Phe)	rs587777492
NM_021072.4(HCN1):c.459G>C (p.Met153Ile)	rs1057519548
NM_021072.4(HCN1):c.469C>G (p.Leu157Val)	rs1561230606
NM_021072.4(HCN1):c.585G>T (p.Arg195Ser)
NM_021072.4(HCN1):c.701A>T (p.Tyr234Phe)	rs1554037381
NM_021072.4(HCN1):c.728T>G (p.Met243Arg)	rs1561230486
NM_021072.4(HCN1):c.814T>C (p.Ser272Pro)	rs587777493
NM_021072.4(HCN1):c.835C>T (p.His279Tyr)	rs587777495
NM_021072.4(HCN1):c.890G>C (p.Arg297Thr)	rs587777494
NM_021072.4(HCN1):c.913A>T (p.Met305Leu)	rs1057521989
NM_021072.4(HCN1):c.986G>C (p.Cys329Ser)	rs1318391259

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