List of variants in gene KCNQ4 reported as likely pathogenic for perceptual disorders

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_004700.4(KCNQ4):c.961G>A (p.Gly321Ser)	rs28939710	0.00001
NM_004700.4(KCNQ4):c.1107T>A (p.Tyr369Ter)
NM_004700.4(KCNQ4):c.1251del (p.Cys418fs)	rs2148324207
NM_004700.4(KCNQ4):c.1438C>T (p.Gln480Ter)	rs1648636515
NM_004700.4(KCNQ4):c.1668C>G (p.Tyr556Ter)
NM_004700.4(KCNQ4):c.364C>T (p.Gln122Ter)
NM_004700.4(KCNQ4):c.721G>C (p.Ala241Pro)
NM_004700.4(KCNQ4):c.733G>A (p.Gly245Arg)
NM_004700.4(KCNQ4):c.825G>C (p.Trp275Cys)	rs956666801
NM_004700.4(KCNQ4):c.826T>C (p.Trp276Arg)	rs2148319465
NM_004700.4(KCNQ4):c.857A>C (p.Tyr286Ser)	rs876657841
NM_004700.4(KCNQ4):c.859G>A (p.Gly287Ser)	rs137853969
NM_004700.4(KCNQ4):c.872C>T (p.Pro291Leu)	rs797044970
NM_004700.4(KCNQ4):c.882G>A (p.Trp294Ter)

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