"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "KCNQ1OT1"[ - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1879153	NM_000218.3(KCNQ1):c.1393+19784dup	KCNQ1, KCNQ1OT1	Duplication (intron variant)	KCNQ1-related condition +1 more	GBenign/Likely benign
Select item 2641363	NM_000218.3(KCNQ1):c.1393+20618A>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	KCNQ1-related condition +1 more	GBenign/Likely benign
Select item 1701154	NM_000218.3(KCNQ1):c.1393+20645G>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879154	NM_000218.3(KCNQ1):c.1393+20735_1393+20738del	KCNQ1, KCNQ1OT1	Microsatellite (intron variant)	not provided	GBenign
Select item 1711272	NM_000218.3(KCNQ1):c.1393+21257T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641364	NM_000218.3(KCNQ1):c.1393+21480C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641365	NM_000218.3(KCNQ1):c.1393+21883_1393+21891del	KCNQ1, KCNQ1OT1	Deletion (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2582883	NM_000218.3(KCNQ1):c.1393+21881_1393+21891del	KCNQ1, KCNQ1OT1	Deletion (intron variant)	not provided	GBenign
Select item 1879155	NM_000218.3(KCNQ1):c.1393+22149A>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	KCNQ1-related condition +1 more	GBenign/Likely benign
Select item 2498481	NM_000218.3(KCNQ1):c.1393+22394C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1694588	NM_000218.3(KCNQ1):c.1393+22427G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641366	NM_000218.3(KCNQ1):c.1393+22468C>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641367	NM_000218.3(KCNQ1):c.1393+23352T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641368	NM_000218.3(KCNQ1):c.1393+23648_1393+23651del	KCNQ1, KCNQ1OT1	Microsatellite (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 3026400	NM_000218.3(KCNQ1):c.1393+23645C>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641369	NM_000218.3(KCNQ1):c.1393+23747A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641370	NM_000218.3(KCNQ1):c.1393+24102T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879156	NM_000218.3(KCNQ1):c.1393+24215A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1711273	NM_000218.3(KCNQ1):c.1393+24489C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879157	NM_000218.3(KCNQ1):c.1393+24554C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3026383	NM_000218.3(KCNQ1):c.1393+24587A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1694589	NM_000218.3(KCNQ1):c.1393+24722T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2578628	NM_000218.3(KCNQ1):c.1393+25307G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879158	NM_000218.3(KCNQ1):c.1393+25378A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2578629	NM_000218.3(KCNQ1):c.1393+25398C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3026384	NM_000218.3(KCNQ1):c.1393+25752G>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2672440	NM_000218.3(KCNQ1):c.1393+25830A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641371	NM_000218.3(KCNQ1):c.1393+26185T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641372	NM_000218.3(KCNQ1):c.1393+27038_1393+27039del	KCNQ1, KCNQ1OT1	Deletion (non-coding transcript variant +1 more)	not provided	GBenign
Select item 3026385	NM_000218.3(KCNQ1):c.1393+27171A>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641373	NM_000218.3(KCNQ1):c.1393+27282A>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1879159	NM_000218.3(KCNQ1):c.1393+27338G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3026374	NM_000218.3(KCNQ1):c.1393+27378del	KCNQ1, KCNQ1OT1	Deletion (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1694590	NM_000218.3(KCNQ1):c.1393+27384G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641374	NM_000218.3(KCNQ1):c.1393+27732C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2582884	NM_000218.3(KCNQ1):c.1393+28521A>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1694591	NM_000218.3(KCNQ1):c.1393+28622C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641375	NM_000218.3(KCNQ1):c.1393+28822C>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641376	NM_000218.3(KCNQ1):c.1393+29271C>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	KCNQ1-related condition +1 more	GLikely benign
Select item 1879160	NM_000218.3(KCNQ1):c.1393+29461dup	KCNQ1, KCNQ1OT1	Duplication (intron variant)	not provided	GBenign
Select item 2641377	NM_000218.3(KCNQ1):c.1393+29634T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879161	NM_000218.3(KCNQ1):c.1393+29738G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879162	NM_000218.3(KCNQ1):c.1393+29750T>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879163	NM_000218.3(KCNQ1):c.1393+29814G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641378	NM_000218.3(KCNQ1):c.1393+30175C>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879164	NM_000218.3(KCNQ1):c.1393+30231C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879165	NM_000218.3(KCNQ1):c.1393+30256G>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641379	NM_000218.3(KCNQ1):c.1393+30303T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1694592	NM_000218.3(KCNQ1):c.1393+30318T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2570783	NM_000218.3(KCNQ1):c.1393+30401G>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1879166	NM_000218.3(KCNQ1):c.1393+31012T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641380	NM_000218.3(KCNQ1):c.1393+31020A>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 3026409	NM_000218.3(KCNQ1):c.1393+31139G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2570784	NM_000218.3(KCNQ1):c.1393+31188T>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641381	NM_000218.3(KCNQ1):c.1393+31346TA[7]	KCNQ1, KCNQ1OT1	Microsatellite (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879167	NM_000218.3(KCNQ1):c.1393+31358_1393+31359insATT	KCNQ1, KCNQ1OT1	Insertion (intron variant)	not provided	GBenign
Select item 1694593	NM_000218.3(KCNQ1):c.1393+31357del	KCNQ1, KCNQ1OT1	Deletion (intron variant)	not provided	GBenign
Select item 2641382	NM_000218.3(KCNQ1):c.1393+31369del	KCNQ1, KCNQ1OT1	Deletion (intron variant +1 more)	not provided	GBenign
Select item 2641383	NM_000218.3(KCNQ1):c.1393+31362T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641384	NM_000218.3(KCNQ1):c.1393+31363T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641385	NM_000218.3(KCNQ1):c.1393+31365T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1711274	NM_000218.3(KCNQ1):c.1393+31367T>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1701155	NM_000218.3(KCNQ1):c.1393+31864G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1694594	NM_000218.3(KCNQ1):c.1393+32039G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2641386	NM_000218.3(KCNQ1):c.1393+32098_1393+32099insGTT	KCNQ1, KCNQ1OT1	Insertion (non-coding transcript variant +1 more)	not provided	GBenign
Select item 3026345	NM_000218.3(KCNQ1):c.1393+32098_1393+32099insGT	KCNQ1, KCNQ1OT1	Insertion (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1711275	NM_000218.3(KCNQ1):c.1393+32122dup	KCNQ1, KCNQ1OT1	Duplication (intron variant)	not provided +1 more	GLikely benign
Select item 1879168	NM_000218.3(KCNQ1):c.1393+32185G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879169	NM_000218.3(KCNQ1):c.1393+32192C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1879170	NM_000218.3(KCNQ1):c.1393+32716A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3026361	NM_000218.3(KCNQ1):c.1393+32806T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2641387	NM_000218.3(KCNQ1):c.1393+33491_1393+33494del	KCNQ1, KCNQ1OT1	Deletion (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641388	NM_000218.3(KCNQ1):c.1393+33589C>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879171	NM_000218.3(KCNQ1):c.1393+33623A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1711276	NM_000218.3(KCNQ1):c.1393+33832G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1694595	NM_000218.3(KCNQ1):c.1393+33929C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3067765	NM_000218.3(KCNQ1):c.1393+34458G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2641389	NM_000218.3(KCNQ1):c.1393+34464G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2641390	NM_000218.3(KCNQ1):c.1393+34768A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 3026403	NM_000218.3(KCNQ1):c.1393+35192T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2582885	NM_000218.3(KCNQ1):c.1393+35379G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641391	NM_000218.3(KCNQ1):c.1393+35431T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1879172	NM_000218.3(KCNQ1):c.1393+35447T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2498482	NM_000218.3(KCNQ1):c.1393+35888C>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641392	NM_000218.3(KCNQ1):c.1393+35891C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2641393	NM_000218.3(KCNQ1):c.1393+36170A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641394	NM_000218.3(KCNQ1):c.1393+36529G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 2570785	NM_000218.3(KCNQ1):c.1394-36442A>G	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641395	NM_000218.3(KCNQ1):c.1394-36384C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1711277	NM_000218.3(KCNQ1):c.1394-36342del	KCNQ1, KCNQ1OT1	Deletion (intron variant)	not provided	GBenign
Select item 1701156	NM_000218.3(KCNQ1):c.1394-36145G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2578630	NM_000218.3(KCNQ1):c.1394-36112G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2672441	NM_000218.3(KCNQ1):c.1394-35987T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 3067766	NM_000218.3(KCNQ1):c.1394-34811G>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2641396	NM_000218.3(KCNQ1):c.1394-34554C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1694596	NM_000218.3(KCNQ1):c.1394-34447C>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	KCNQ1-related condition +1 more	GLikely benign
Select item 3026355	NM_000218.3(KCNQ1):c.1394-34133G>A	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2641397	NM_000218.3(KCNQ1):c.1394-34090C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1701157	NM_000218.3(KCNQ1):c.1394-33886C>T	KCNQ1, KCNQ1OT1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2641398	NM_000218.3(KCNQ1):c.1394-33375T>C	KCNQ1, KCNQ1OT1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

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