List of variants in gene KCNQ4 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.1188C>T (p.Pro396=)	rs189541861	0.00222
NM_004700.4(KCNQ4):c.465A>C (p.Gly155=)	rs145129529	0.00082
NM_004700.4(KCNQ4):c.438G>A (p.Glu146=)	rs144434662	0.00025
NM_004700.4(KCNQ4):c.419T>C (p.Ile140Thr)	rs200053059	0.00007
NM_004700.4(KCNQ4):c.2006A>G (p.His669Arg)	rs749565877	0.00001
NM_004700.4(KCNQ4):c.2086T>G (p.Ter696Gly)	rs748770400	0.00001
NM_004700.4(KCNQ4):c.1005C>T (p.Phe335=)
NM_004700.4(KCNQ4):c.1012C>T (p.Arg338Trp)	rs2148320413
NM_004700.4(KCNQ4):c.109G>A (p.Gly37Ser)
NM_004700.4(KCNQ4):c.1322G>A (p.Arg441His)
NM_004700.4(KCNQ4):c.1438C>T (p.Gln480Ter)	rs1648636515
NM_004700.4(KCNQ4):c.485G>A (p.Gly162Glu)
NM_004700.4(KCNQ4):c.603C>T (p.Ser201=)
NM_004700.4(KCNQ4):c.840A>G (p.Thr280=)
NM_004700.4(KCNQ4):c.872C>T (p.Pro291Leu)	rs797044970
NM_004700.4(KCNQ4):c.992G>A (p.Arg331Gln)

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