PR:000000920	voltage-gated potassium channel subunit KCNQ4 sequence variant G285C (human)	hKCNQ4/var:G285C|UniProtKB:P56696-1, Gly-285, CHEBI:29950|voltage-gated potassium channel subunit KCNQ4 sequence variant 1 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10369879	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008727	20080601	PRO:CNA	
PR:000000920	voltage-gated potassium channel subunit KCNQ4 sequence variant G285C (human)	hKCNQ4/var:G285C|UniProtKB:P56696-1, Gly-285, CHEBI:29950|voltage-gated potassium channel subunit KCNQ4 sequence variant 1 (human)	altered	capable_of	GO:0005249	voltage-gated potassium channel activity	PR:000000918		PMID:10369879	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008727	20080601	PRO:CNA	
PR:000000921	voltage-gated potassium channel subunit KCNQ4 sequence variant L274H (human)	hKCNQ4/var:L274H|UniProtKB:P56696-1, Leu-274, CHEBI:29979|voltage-gated potassium channel subunit KCNQ4 sequence variant 2 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10925378	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_010936	20080601	PRO:CNA	
PR:000000922	voltage-gated potassium channel subunit KCNQ4 sequence variant G285S (human)	hKCNQ4/var:G285S|UniProtKB:P56696-1, Gly-285, CHEBI:29999|voltage-gated potassium channel subunit KCNQ4 sequence variant 3 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10025409	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_001547	20080601	PRO:CNA	
PR:000000922	voltage-gated potassium channel subunit KCNQ4 sequence variant G285S (human)	hKCNQ4/var:G285S|UniProtKB:P56696-1, Gly-285, CHEBI:29999|voltage-gated potassium channel subunit KCNQ4 sequence variant 3 (human)	altered	capable_of	GO:0005249	voltage-gated potassium channel activity	PR:000000918		PMID:10025409	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_001547	20080601	PRO:CNA	
PR:000000923	voltage-gated potassium channel subunit KCNQ4 sequence variant L281S (human)	hKCNQ4/var:L281S|UniProtKB:P56696-1, Leu-281, CHEBI:29999|voltage-gated potassium channel subunit KCNQ4 sequence variant 4 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10571947	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_010937	20080601	PRO:CNA	
PR:000000924	voltage-gated potassium channel subunit KCNQ4 sequence variant W276S (human)	hKCNQ4/var:W276S|UniProtKB:P56696-1, Trp-276, CHEBI:29999|voltage-gated potassium channel subunit KCNQ4 sequence variant 5 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10369879	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008726	20080601	PRO:CNA	
PR:000000925	voltage-gated potassium channel subunit KCNQ4 sequence variant G321S (human)	hKCNQ4/var:G321S|UniProtKB:P56696-1, Gly-321, CHEBI:29999|voltage-gated potassium channel subunit KCNQ4 sequence variant 6 (human)		associated_with_disease_progression	DOID:0050564	autosomal dominant nonsyndromic deafness			PMID:10369879	EXP	NCBITaxon:9606		UniProtKB_VAR:VAR_008728	20080601	PRO:CNA