Product Details

Primer Sequences

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Primer Chromosome Location

Chr.8: 109968210-109968435 on Build GRCh38 View in UCSC browser

Format

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer^™ Tool Quick Reference

Ampliseq ID's

Gene Details

Gene Symbol

KCNV1

Entrez Gene ID

27012

Gene Name

potassium voltage-gated channel modifier subfamily V member 1

Gene Aliases

HNKA, KCNB3, KV2.3, KV8.1

UniGene

Hs.13285

Gene Chromosome Location

Chr.8: 109963645-109975847 on Build GRCh38

Transcripts

NM_014379.3

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
3162978	c.1289G>A	p.R430H	Chr.8: 109968302-109968302 on Build GRCh38
1094998	c.1252C>T	p.L418F	Chr.8: 109968339-109968339 on Build GRCh38
3162979	c.1285G>A	p.D429N	Chr.8: 109968306-109968306 on Build GRCh38
3951145	c.1225G>A	p.A409T	Chr.8: 109968366-109968366 on Build GRCh38
4694760	c.1362T>C	p.L454L	Chr.8: 109968229-109968229 on Build GRCh38
748744	c.1221C>T	p.I407I	Chr.8: 109968370-109968370 on Build GRCh38
6691956	c.1275T>C	p.A425A	Chr.8: 109968316-109968316 on Build GRCh38
748745	c.1280T>C	p.I427T	Chr.8: 109968311-109968311 on Build GRCh38
6111944	c.1273G>C	p.A425P	Chr.8: 109968318-109968318 on Build GRCh38
3924500	c.1356G>A	p.K452K	Chr.8: 109968235-109968235 on Build GRCh38
3924501	c.1324G>A	p.E442K	Chr.8: 109968267-109968267 on Build GRCh38
748746	c.1368G>C	p.K456N	Chr.8: 109968223-109968223 on Build GRCh38
3644123	c.1323G>A	p.K441K	Chr.8: 109968268-109968268 on Build GRCh38
3644124	c.1284C>T	p.N428N	Chr.8: 109968307-109968307 on Build GRCh38
3644125	c.1247G>A	p.G416E	Chr.8: 109968344-109968344 on Build GRCh38
453867	c.1245G>A	p.S415S	Chr.8: 109968346-109968346 on Build GRCh38
6691954	c.1219_1220insA	p.I407fs*22	Chr.8: 109968371-109968372 on Build GRCh38
3884756	c.1156G>A	p.A386T	Chr.8: 109968435-109968435 on Build GRCh38
7427438	c.1269T>A	p.P423P	Chr.8: 109968322-109968322 on Build GRCh38
7447683	c.1253T>G	p.L418R	Chr.8: 109968338-109968338 on Build GRCh38
1255457	c.1351C>A	p.L451I	Chr.8: 109968240-109968240 on Build GRCh38
3884752	c.1337G>C	p.R446T	Chr.8: 109968254-109968254 on Build GRCh38
1211667	c.1342C>T	p.R448C	Chr.8: 109968249-109968249 on Build GRCh38
4451684	c.1354A>G	p.K452E	Chr.8: 109968237-109968237 on Build GRCh38
1700472	c.1348G>A	p.A450T	Chr.8: 109968243-109968243 on Build GRCh38
3884753	c.1306T>G	p.F436V	Chr.8: 109968285-109968285 on Build GRCh38
6490300	c.1183T>A	p.Y395N	Chr.8: 109968408-109968408 on Build GRCh38
3884754	c.1271T>A	p.I424N	Chr.8: 109968320-109968320 on Build GRCh38
3358196	c.1261G>A	p.A421T	Chr.8: 109968330-109968330 on Build GRCh38
4465060	c.1365C>T	p.T455T	Chr.8: 109968226-109968226 on Build GRCh38
3884755	c.1267C>T	p.P423S	Chr.8: 109968324-109968324 on Build GRCh38
5791468	c.1244C>T	p.S415L	Chr.8: 109968347-109968347 on Build GRCh38
3785849	c.1334T>A	p.V445D	Chr.8: 109968257-109968257 on Build GRCh38
1176612	c.1288C>T	p.R430C	Chr.8: 109968303-109968303 on Build GRCh38
6476627	c.1255G>C	p.V419L	Chr.8: 109968336-109968336 on Build GRCh38
421773	c.1376C>A	p.A459D	Chr.8: 109968215-109968215 on Build GRCh38
4876733	c.1347A>T	p.E449D	Chr.8: 109968244-109968244 on Build GRCh38
5716020	c.1323G>T	p.K441N	Chr.8: 109968268-109968268 on Build GRCh38
1196328	c.1255G>T	p.V419F	Chr.8: 109968336-109968336 on Build GRCh38
4399432	c.1351C>T	p.L451L	Chr.8: 109968240-109968240 on Build GRCh38
5669213	c.1336A>G	p.R446G	Chr.8: 109968255-109968255 on Build GRCh38
4149497	c.1206C>T	p.T402T	Chr.8: 109968385-109968385 on Build GRCh38
1094999	c.1157C>T	p.A386V	Chr.8: 109968434-109968434 on Build GRCh38
5591480	c.1381G>A	p.D461N	Chr.8: 109968210-109968210 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs201081474	Chr.8: 109968346-109968346 on Build GRCh38
rs781447839	Chr.8: 109968360-109968360 on Build GRCh38
rs757610737	Chr.8: 109968349-109968349 on Build GRCh38
rs190126683	Chr.8: 109968334-109968334 on Build GRCh38
rs988600153	Chr.8: 109968279-109968279 on Build GRCh38
rs538554637	Chr.8: 109968253-109968253 on Build GRCh38
rs751431090	Chr.8: 109968248-109968248 on Build GRCh38
rs752727710	Chr.8: 109968314-109968314 on Build GRCh38
rs747595000	Chr.8: 109968383-109968383 on Build GRCh38
rs568696386	Chr.8: 109968364-109968364 on Build GRCh38
rs770730541	Chr.8: 109968406-109968406 on Build GRCh38
rs780641862	Chr.8: 109968379-109968379 on Build GRCh38
rs771722330	Chr.8: 109968393-109968393 on Build GRCh38
rs866800552	Chr.8: 109968267-109968267 on Build GRCh38
rs765340856	Chr.8: 109968307-109968307 on Build GRCh38
rs756527587	Chr.8: 109968370-109968370 on Build GRCh38
rs758508412	Chr.8: 109968328-109968328 on Build GRCh38
rs776341934	Chr.8: 109968412-109968412 on Build GRCh38
rs371299964	Chr.8: 109968258-109968258 on Build GRCh38
rs139725290	Chr.8: 109968403-109968403 on Build GRCh38
rs377331545	Chr.8: 109968280-109968280 on Build GRCh38
rs748736647	Chr.8: 109968391-109968391 on Build GRCh38
rs772986756	Chr.8: 109968396-109968396 on Build GRCh38
rs944340597	Chr.8: 109968281-109968281 on Build GRCh38

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