Product Details

Primer Sequences

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Primer Chromosome Location

Chr.1: 203699545-203699788 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

ATP2B4

Entrez Gene ID

493

Gene Name

ATPase plasma membrane Ca2+ transporting 4

Gene Aliases

ATP2B2, MXRA1, PMCA4, PMCA4b, PMCA4x

UniGene

Hs.343522

Gene Chromosome Location

Chr.1: 203626787-203744081 on Build GRCh38

Transcripts

NM_001001396.2 NM_001684.4

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
902495	c.648C>T	p.Y216Y	Chr.1: 203699716-203699716 on Build GRCh38
159275	c.522G>C	p.E174D	Chr.1: 203699590-203699590 on Build GRCh38
4664385	c.581G>A	p.R194Q	Chr.1: 203699649-203699649 on Build GRCh38
6124133	c.483C>T	p.I161I	Chr.1: 203699551-203699551 on Build GRCh38
463787	c.546C>T	p.C182C	Chr.1: 203699614-203699614 on Build GRCh38
7132839	c.513G>C	p.W171C	Chr.1: 203699581-203699581 on Build GRCh38
6607810	c.533G>A	p.R178Q	Chr.1: 203699601-203699601 on Build GRCh38
6341168	c.586G>T	p.G196C	Chr.1: 203699654-203699654 on Build GRCh38
7135831	c.477G>T	p.V159V	Chr.1: 203699545-203699545 on Build GRCh38
6124132	c.483C>T	p.I161I	Chr.1: 203699551-203699551 on Build GRCh38
6607817	c.635C>T	p.A212V	Chr.1: 203699703-203699703 on Build GRCh38
2213787	c.547C>T	p.R183C	Chr.1: 203699615-203699615 on Build GRCh38
902494	c.582delA	p.N195fs*32	Chr.1: 203699650-203699650 on Build GRCh38
2213786	c.532C>T	p.R178W	Chr.1: 203699600-203699600 on Build GRCh38
4027192	c.491T>A	p.L164*	Chr.1: 203699559-203699559 on Build GRCh38
1184085	c.604C>T	p.P202S	Chr.1: 203699672-203699672 on Build GRCh38
6607816	c.635C>T	p.A212V	Chr.1: 203699703-203699703 on Build GRCh38
3803525	c.587G>C	p.G196A	Chr.1: 203699655-203699655 on Build GRCh38
4664386	c.581G>A	p.R194Q	Chr.1: 203699649-203699649 on Build GRCh38
3481885	c.570C>T	p.F190F	Chr.1: 203699638-203699638 on Build GRCh38
7263997	c.542A>G	p.Q181R	Chr.1: 203699610-203699610 on Build GRCh38
5934230	c.572C>T	p.S191F	Chr.1: 203699640-203699640 on Build GRCh38
1338009	c.529delT	p.F177fs*50	Chr.1: 203699597-203699597 on Build GRCh38
7166430	c.480C>G	p.I160M	Chr.1: 203699548-203699548 on Build GRCh38
4664383	c.574A>G	p.I192V	Chr.1: 203699642-203699642 on Build GRCh38
4823380	c.594C>T	p.L198L	Chr.1: 203699662-203699662 on Build GRCh38
6607811	c.533G>A	p.R178Q	Chr.1: 203699601-203699601 on Build GRCh38
3803524	c.587G>C	p.G196A	Chr.1: 203699655-203699655 on Build GRCh38
902493	c.582delA	p.N195fs*32	Chr.1: 203699650-203699650 on Build GRCh38
7135832	c.477G>T	p.V159V	Chr.1: 203699545-203699545 on Build GRCh38
5558701	c.492A>T	p.L164F	Chr.1: 203699560-203699560 on Build GRCh38
4764414	c.649G>A	p.G217S	Chr.1: 203699717-203699717 on Build GRCh38
3481884	c.570C>T	p.F190F	Chr.1: 203699638-203699638 on Build GRCh38
7132838	c.513G>C	p.W171C	Chr.1: 203699581-203699581 on Build GRCh38
219547	c.522G>C	p.E174D	Chr.1: 203699590-203699590 on Build GRCh38
1184084	c.604C>T	p.P202S	Chr.1: 203699672-203699672 on Build GRCh38
4823379	c.594C>T	p.L198L	Chr.1: 203699662-203699662 on Build GRCh38
7263998	c.542A>G	p.Q181R	Chr.1: 203699610-203699610 on Build GRCh38
4764413	c.649G>A	p.G217S	Chr.1: 203699717-203699717 on Build GRCh38
4027193	c.491T>A	p.L164*	Chr.1: 203699559-203699559 on Build GRCh38
6341167	c.586G>T	p.G196C	Chr.1: 203699654-203699654 on Build GRCh38
902496	c.648C>T	p.Y216Y	Chr.1: 203699716-203699716 on Build GRCh38
2213785	c.532C>T	p.R178W	Chr.1: 203699600-203699600 on Build GRCh38
5934231	c.572C>T	p.S191F	Chr.1: 203699640-203699640 on Build GRCh38
4229510	c.580C>T	p.R194*	Chr.1: 203699648-203699648 on Build GRCh38
7166429	c.480C>G	p.I160M	Chr.1: 203699548-203699548 on Build GRCh38
2213788	c.547C>T	p.R183C	Chr.1: 203699615-203699615 on Build GRCh38
4664384	c.574A>G	p.I192V	Chr.1: 203699642-203699642 on Build GRCh38
463788	c.546C>T	p.C182C	Chr.1: 203699614-203699614 on Build GRCh38
5558702	c.492A>T	p.L164F	Chr.1: 203699560-203699560 on Build GRCh38
4229509	c.580C>T	p.R194*	Chr.1: 203699648-203699648 on Build GRCh38
1338008	c.529delT	p.F177fs*50	Chr.1: 203699597-203699597 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs373246108	Chr.1: 203699575-203699575 on Build GRCh38
rs6680050	Chr.1: 203699623-203699623 on Build GRCh38
rs1005725066	Chr.1: 203699635-203699635 on Build GRCh38
rs199621401	Chr.1: 203699616-203699616 on Build GRCh38
rs75737190	Chr.1: 203699762-203699762 on Build GRCh38
rs775969773	Chr.1: 203699749-203699749 on Build GRCh38
rs779807808	Chr.1: 203699654-203699654 on Build GRCh38
rs148661659	Chr.1: 203699658-203699658 on Build GRCh38
rs749104124	Chr.1: 203699686-203699686 on Build GRCh38
rs780709781	Chr.1: 203699648-203699648 on Build GRCh38
rs746075249	Chr.1: 203699746-203699746 on Build GRCh38
rs372840559	Chr.1: 203699760-203699760 on Build GRCh38
rs150802414	Chr.1: 203699629-203699629 on Build GRCh38
rs748137308	Chr.1: 203699716-203699716 on Build GRCh38
rs770208103	Chr.1: 203699747-203699747 on Build GRCh38
rs966048307	Chr.1: 203699717-203699717 on Build GRCh38
rs377304100	Chr.1: 203699729-203699729 on Build GRCh38
rs998689356	Chr.1: 203699690-203699690 on Build GRCh38
rs753169842	Chr.1: 203699605-203699605 on Build GRCh38
rs759843418	Chr.1: 203699600-203699600 on Build GRCh38
rs374733543	Chr.1: 203699615-203699615 on Build GRCh38
rs771160051	Chr.1: 203699589-203699589 on Build GRCh38
rs778763585	Chr.1: 203699706-203699706 on Build GRCh38
rs756675985	Chr.1: 203699631-203699631 on Build GRCh38
rs370813276	Chr.1: 203699761-203699761 on Build GRCh38
rs776954727	Chr.1: 203699594-203699594 on Build GRCh38
rs750008040	Chr.1: 203699649-203699649 on Build GRCh38
rs375257658	Chr.1: 203699728-203699728 on Build GRCh38
rs200574191	Chr.1: 203699756-203699756 on Build GRCh38
rs149951732	Chr.1: 203699653-203699653 on Build GRCh38
rs765639720	Chr.1: 203699601-203699601 on Build GRCh38
rs768606063	Chr.1: 203699703-203699703 on Build GRCh38

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