Product Details

Primer Sequences

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Primer Chromosome Location

Chr.4: 20749563-20749836 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

KCNIP4

Entrez Gene ID

80333

Gene Name

potassium voltage-gated channel interacting protein 4

Gene Aliases

CALP, KCHIP4

UniGene

Hs.655705

Gene Chromosome Location

Chr.4: 20728520-21948801 on Build GRCh38

Transcripts

NM_001035003.1 NM_001035004.1 NM_025221.5 NM_147181.3 NM_147182.3 NM_147183.3 XM_005248190.4 XM_011513882.2 XM_011513883.2 XM_011513884.2 XM_011513885.2 XM_011513886.2 XM_011513887.2 XM_011513889.2 XM_017008653.1 NR_133933.1

Gene Symbol

PACRGL

Entrez Gene ID

133015

Gene Name

PARK2 coregulated like

Gene Aliases

C4orf28

UniGene

Hs.479298

Gene Chromosome Location

Chr.4: 20696282-20757766 on Build GRCh38

Transcripts

NM_001035003.1 NM_001035004.1 NM_025221.5 NM_147181.3 NM_147182.3 NM_147183.3 XM_005248190.4 XM_011513882.2 XM_011513883.2 XM_011513884.2 XM_011513885.2 XM_011513886.2 XM_011513887.2 XM_011513889.2 XM_017008653.1 NR_133933.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
3132626	c.337A>G	p.T113A	Chr.4: 20749691-20749691 on Build GRCh38
3373467	c.310T>G	p.F104V	Chr.4: 20749706-20749706 on Build GRCh38
7401404	c.397G>A	p.D133N	Chr.4: 20749694-20749694 on Build GRCh38
5060305	c.354T>C	p.A118A	Chr.4: 20749674-20749674 on Build GRCh38
1753682	c.420G>A	p.V140V	Chr.4: 20749671-20749671 on Build GRCh38
5060304	c.417T>C	p.A139A	Chr.4: 20749674-20749674 on Build GRCh38
733717	c.366+1G>A	p.?	Chr.4: 20749661-20749661 on Build GRCh38
1594525	c.426C>T	p.F142F	Chr.4: 20749665-20749665 on Build GRCh38
299274	c.363C>T	p.F121F	Chr.4: 20749665-20749665 on Build GRCh38
6427195	c.280C>G	p.L94V	Chr.4: 20749709-20749709 on Build GRCh38
5700517	c.312C>A	p.F104L	Chr.4: 20749704-20749704 on Build GRCh38
1149910	c.354+1G>A	p.?	Chr.4: 20749661-20749661 on Build GRCh38
3373465	c.385T>G	p.F129V	Chr.4: 20749706-20749706 on Build GRCh38
3132625	c.400A>G	p.T134A	Chr.4: 20749691-20749691 on Build GRCh38
6427194	c.307C>G	p.L103V	Chr.4: 20749709-20749709 on Build GRCh38
7401405	c.334G>A	p.D112N	Chr.4: 20749694-20749694 on Build GRCh38
5466127	c.319C>A	p.L107M	Chr.4: 20749709-20749709 on Build GRCh38
4417394	c.327+7T>C	p.?	Chr.4: 20749655-20749655 on Build GRCh38
3373466	c.322T>G	p.F108V	Chr.4: 20749706-20749706 on Build GRCh38
5466126	c.382C>A	p.L128M	Chr.4: 20749709-20749709 on Build GRCh38
3132628	c.298A>G	p.T100A	Chr.4: 20749691-20749691 on Build GRCh38
6427192	c.382C>G	p.L128V	Chr.4: 20749709-20749709 on Build GRCh38
7401406	c.322G>A	p.D108N	Chr.4: 20749694-20749694 on Build GRCh38
6427193	c.319C>G	p.L107V	Chr.4: 20749709-20749709 on Build GRCh38
1149909	c.429+1G>A	p.?	Chr.4: 20749661-20749661 on Build GRCh38
1594526	c.351C>T	p.F117F	Chr.4: 20749665-20749665 on Build GRCh38
733718	c.327+1G>A	p.?	Chr.4: 20749661-20749661 on Build GRCh38
5700516	c.324C>A	p.F108L	Chr.4: 20749704-20749704 on Build GRCh38
5700515	c.387C>A	p.F129L	Chr.4: 20749704-20749704 on Build GRCh38
1753685	c.318G>A	p.V106V	Chr.4: 20749671-20749671 on Build GRCh38
7401407	c.295G>A	p.D99N	Chr.4: 20749694-20749694 on Build GRCh38
5060307	c.315T>C	p.A105A	Chr.4: 20749674-20749674 on Build GRCh38
299275	c.324C>T	p.F108F	Chr.4: 20749665-20749665 on Build GRCh38
4417393	c.354+7T>C	p.?	Chr.4: 20749655-20749655 on Build GRCh38
5466128	c.307C>A	p.L103M	Chr.4: 20749709-20749709 on Build GRCh38
1753684	c.345G>A	p.V115V	Chr.4: 20749671-20749671 on Build GRCh38
5700518	c.285C>A	p.F95L	Chr.4: 20749704-20749704 on Build GRCh38
4417391	c.429+7T>C	p.?	Chr.4: 20749655-20749655 on Build GRCh38
1753683	c.357G>A	p.V119V	Chr.4: 20749671-20749671 on Build GRCh38
3132627	c.325A>G	p.T109A	Chr.4: 20749691-20749691 on Build GRCh38
5466129	c.280C>A	p.L94M	Chr.4: 20749709-20749709 on Build GRCh38
5060306	c.342T>C	p.A114A	Chr.4: 20749674-20749674 on Build GRCh38
4417392	c.366+7T>C	p.?	Chr.4: 20749655-20749655 on Build GRCh38
3373468	c.283T>G	p.F95V	Chr.4: 20749706-20749706 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs780303241	Chr.4: 20749613-20749613 on Build GRCh38
rs2322688	Chr.4: 20749655-20749655 on Build GRCh38
rs777091293	Chr.4: 20749653-20749653 on Build GRCh38
rs756779365	Chr.4: 20749680-20749680 on Build GRCh38
rs374097995	Chr.4: 20749741-20749741 on Build GRCh38
rs772509553	Chr.4: 20749627-20749627 on Build GRCh38
rs750337453	Chr.4: 20749691-20749691 on Build GRCh38
rs112653243	Chr.4: 20749783-20749783 on Build GRCh38
rs932421345	Chr.4: 20749768-20749768 on Build GRCh38
rs749012604	Chr.4: 20749722-20749722 on Build GRCh38
rs73802309	Chr.4: 20749597-20749597 on Build GRCh38
rs768879714	Chr.4: 20749615-20749615 on Build GRCh38
rs767393802	Chr.4: 20749681-20749681 on Build GRCh38
rs748240446	Chr.4: 20749764-20749764 on Build GRCh38
rs763735612	Chr.4: 20749656-20749656 on Build GRCh38
rs779855024	Chr.4: 20749719-20749719 on Build GRCh38
rs370308743	Chr.4: 20749636-20749636 on Build GRCh38
rs1049471516	Chr.4: 20749776-20749776 on Build GRCh38
rs757747371	Chr.4: 20749798-20749798 on Build GRCh38
rs761164144	Chr.4: 20749641-20749641 on Build GRCh38
rs779180133	Chr.4: 20749757-20749757 on Build GRCh38
rs755996521	Chr.4: 20749706-20749706 on Build GRCh38
rs772163502	Chr.4: 20749781-20749781 on Build GRCh38
rs774295683	Chr.4: 20749616-20749616 on Build GRCh38
rs773853961	Chr.4: 20749635-20749635 on Build GRCh38
rs922388861	Chr.4: 20749743-20749743 on Build GRCh38
rs369759324	Chr.4: 20749608-20749608 on Build GRCh38
rs751047200	Chr.4: 20749665-20749665 on Build GRCh38
rs949696688	Chr.4: 20749807-20749807 on Build GRCh38
rs749534148	Chr.4: 20749614-20749614 on Build GRCh38
rs748198574	Chr.4: 20749623-20749623 on Build GRCh38
rs953784613	Chr.4: 20749740-20749740 on Build GRCh38
rs766832653	Chr.4: 20749644-20749644 on Build GRCh38
rs764506120	Chr.4: 20749772-20749772 on Build GRCh38

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