KCNQ3[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 361745	NM_004519.4(KCNQ3):c.*8148G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 911262	NM_004519.4(KCNQ3):c.*8102G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361746	NM_004519.4(KCNQ3):c.*7980dup	KCNQ3	Duplication (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GUncertain significance
Select item 911263	NM_004519.4(KCNQ3):c.*7923G>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361747	NM_004519.4(KCNQ3):c.*7722T>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 361748	NM_004519.4(KCNQ3):c.*7689A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign/Likely benign
Select item 361749	NM_004519.4(KCNQ3):c.*7512T>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GUncertain significance
Select item 361750	NM_004519.4(KCNQ3):c.*7506C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361751	NM_004519.4(KCNQ3):c.*7504C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign/Likely benign
Select item 361752	NM_004519.4(KCNQ3):c.*7464C>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign/Likely benign
Select item 911460	NM_004519.4(KCNQ3):c.*7461G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 361753	NM_004519.4(KCNQ3):c.*7413G>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign/Likely benign
Select item 911461	NM_004519.4(KCNQ3):c.*7408G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361754	NM_004519.4(KCNQ3):c.*7371T>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign
Select item 361755	NM_004519.4(KCNQ3):c.*7331A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GConflicting classifications of pathogenicity
Select item 361756	NM_004519.4(KCNQ3):c.*7243C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361757	NM_004519.4(KCNQ3):c.*7221C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361758	NM_004519.4(KCNQ3):c.*7214G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 908485	NM_004519.4(KCNQ3):c.*7204G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 908486	NM_004519.4(KCNQ3):c.*7160C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361759	NM_004519.4(KCNQ3):c.*7143A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361760	NM_004519.4(KCNQ3):c.*7131G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 908487	NM_004519.4(KCNQ3):c.*7130C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 361761	NM_004519.4(KCNQ3):c.*7119C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 361762	NM_004519.4(KCNQ3):c.*7095T>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign
Select item 361763	NM_004519.4(KCNQ3):c.*7075A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 909338	NM_004519.4(KCNQ3):c.*7044C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361764	NM_004519.4(KCNQ3):c.*7033T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361765	NM_004519.4(KCNQ3):c.*7015G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361766	NM_004519.4(KCNQ3):c.*6956A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 909339	NM_004519.4(KCNQ3):c.*6913A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361767	NM_004519.4(KCNQ3):c.*6874C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 361768	NM_004519.4(KCNQ3):c.*6831G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GConflicting classifications of pathogenicity
Select item 361769	NM_004519.4(KCNQ3):c.*6812A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 910303	NM_004519.4(KCNQ3):c.*6725A>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 910304	NM_004519.4(KCNQ3):c.*6665A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361770	NM_004519.4(KCNQ3):c.*6632T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361771	NM_004519.4(KCNQ3):c.*6607A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GUncertain significance
Select item 361772	NM_004519.4(KCNQ3):c.*6461G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361773	NM_004519.4(KCNQ3):c.*6460C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GUncertain significance
Select item 910305	NM_004519.4(KCNQ3):c.*6455G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361774	NM_004519.4(KCNQ3):c.*6446del	KCNQ3	Deletion (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GLikely benign
Select item 910306	NM_004519.4(KCNQ3):c.*6384A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 911518	NM_004519.4(KCNQ3):c.*6359C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361775	NM_004519.4(KCNQ3):c.*6351A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361776	NM_004519.4(KCNQ3):c.*6340G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 361777	NM_004519.4(KCNQ3):c.*6282A>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361778	NM_004519.4(KCNQ3):c.*6267T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GConflicting classifications of pathogenicity
Select item 361779	NM_004519.4(KCNQ3):c.*6238T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 361780	NM_004519.4(KCNQ3):c.*6205G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361781	NM_004519.4(KCNQ3):c.*6199C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 361782	NM_004519.4(KCNQ3):c.*6174A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 908555	NM_004519.4(KCNQ3):c.*6142T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 1701556	NM_004519.4(KCNQ3):c.*6046G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 908556	NM_004519.4(KCNQ3):c.*6042A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 908557	NM_004519.4(KCNQ3):c.*6035G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 908558	NM_004519.4(KCNQ3):c.*5971C>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 361783	NM_004519.4(KCNQ3):c.*5965T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign/Likely benign
Select item 361784	NM_004519.4(KCNQ3):c.*5932A>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361785	NM_004519.4(KCNQ3):c.*5762G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign/Likely benign
Select item 361786	NM_004519.4(KCNQ3):c.*5761C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GUncertain significance
Select item 361787	NM_004519.4(KCNQ3):c.*5719C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361788	NM_004519.4(KCNQ3):c.*5704C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 909419	NM_004519.4(KCNQ3):c.*5622C>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361789	NM_004519.4(KCNQ3):c.*5580G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GUncertain significance
Select item 361790	NM_004519.4(KCNQ3):c.*5578A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign/Likely benign
Select item 361791	NM_004519.4(KCNQ3):c.*5521C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GUncertain significance
Select item 361792	NM_004519.4(KCNQ3):c.*5482A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 361793	NM_004519.4(KCNQ3):c.*5466T>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 910365	NM_004519.4(KCNQ3):c.*5454T>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 910366	NM_004519.4(KCNQ3):c.*5423T>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361794	NM_004519.4(KCNQ3):c.*5391C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 910367	NM_004519.4(KCNQ3):c.*5369G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361795	NM_004519.4(KCNQ3):c.*5255T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 361796	NM_004519.4(KCNQ3):c.*5018C>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign neonatal seizures +1 more	GBenign/Likely benign
Select item 910368	NM_004519.4(KCNQ3):c.*5004G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 910369	NM_004519.4(KCNQ3):c.*4983T>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361798	NM_004519.4(KCNQ3):c.*4982A>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GBenign
Select item 361797	NM_004519.4(KCNQ3):c.*4982del	KCNQ3	Deletion (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GBenign
Select item 361799	NM_004519.4(KCNQ3):c.*4958A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 361800	NM_004519.4(KCNQ3):c.*4949G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GConflicting classifications of pathogenicity
Select item 911582	NM_004519.4(KCNQ3):c.*4947G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 911581	NM_004519.4(KCNQ3):c.*4947G>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 361801	NM_004519.4(KCNQ3):c.*4817G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign/Likely benign
Select item 911583	NM_004519.4(KCNQ3):c.*4816C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 908626	NM_004519.4(KCNQ3):c.*4795A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361802	NM_004519.4(KCNQ3):c.4746_4747insACAG	KCNQ3	Insertion (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GBenign
Select item 361803	NM_004519.4(KCNQ3):c.*4736G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign
Select item 361804	NM_004519.4(KCNQ3):c.*4551T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GConflicting classifications of pathogenicity
Select item 908627	NM_004519.4(KCNQ3):c.*4484G>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361805	NM_004519.4(KCNQ3):c.*4481C>A	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GUncertain significance
Select item 361806	NM_004519.4(KCNQ3):c.*4479C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GUncertain significance
Select item 908628	NM_004519.4(KCNQ3):c.*4456A>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 361807	NM_004519.4(KCNQ3):c.*4316del	KCNQ3	Deletion (3 prime UTR variant)	Benign Neonatal Epilepsy +1 more	GLikely benign
Select item 908629	NM_004519.4(KCNQ3):c.*4279C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GBenign
Select item 361808	NM_004519.4(KCNQ3):c.*4258T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign/Likely benign
Select item 361809	NM_004519.4(KCNQ3):c.*4243A>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	not provided +2 more	GBenign
Select item 361810	NM_004519.4(KCNQ3):c.*4125T>C	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +2 more	GBenign
Select item 909488	NM_004519.4(KCNQ3):c.*4122A>G	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2	GUncertain significance
Select item 361811	NM_004519.4(KCNQ3):c.*4043C>T	KCNQ3	Single nucleotide variant (3 prime UTR variant)	Seizures, benign familial neonatal, 2 +1 more	GBenign/Likely benign

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