Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.12: 89603080-89603337 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: ATP2B1
Entrez Gene ID: 490
Gene Name: ATPase plasma membrane Ca2+ transporting 1
Gene Aliases: PMCA1, PMCA1kb
UniGene: Hs.506276
Gene Chromosome Location: Chr.12: 89588049-89709353 on Build GRCh38
Transcripts: NM_001001323.1 NM_001682.2 XM_011538407.2 XM_017019357.1 XM_017019358.1 XM_017019359.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
431963	c.3007A>G	p.I1003V	Chr.12: 89603096-89603096 on Build GRCh38
6607592	c.2958C>T	p.N986N	Chr.12: 89603145-89603145 on Build GRCh38
5587247	c.3001G>A	p.E1001K	Chr.12: 89603102-89603102 on Build GRCh38
3772746	c.2971C>T	p.R991W	Chr.12: 89603132-89603132 on Build GRCh38
6355759	c.2959G>A	p.E987K	Chr.12: 89603144-89603144 on Build GRCh38
3813169	c.2947C>T	p.Q983*	Chr.12: 89603156-89603156 on Build GRCh38
1586795	c.3009C>A	p.I1003I	Chr.12: 89603094-89603094 on Build GRCh38
944304	c.3009C>A	p.I1003I	Chr.12: 89603094-89603094 on Build GRCh38
3813168	c.2947C>T	p.Q983*	Chr.12: 89603156-89603156 on Build GRCh38
1476987	c.3007A>G	p.I1003V	Chr.12: 89603096-89603096 on Build GRCh38
6355760	c.2959G>A	p.E987K	Chr.12: 89603144-89603144 on Build GRCh38
4045307	c.2997A>T	p.V999V	Chr.12: 89603106-89603106 on Build GRCh38
1706009	c.2962A>T	p.I988L	Chr.12: 89603141-89603141 on Build GRCh38
3793025	c.3009C>T	p.I1003I	Chr.12: 89603094-89603094 on Build GRCh38
3955281	c.2869G>C	p.D957H	Chr.12: 89603234-89603234 on Build GRCh38
318835	c.2957A>G	p.N986S	Chr.12: 89603146-89603146 on Build GRCh38
6869717	c.2874T>G	p.S958R	Chr.12: 89603229-89603229 on Build GRCh38
1706010	c.2962A>T	p.I988L	Chr.12: 89603141-89603141 on Build GRCh38
6607593	c.2958C>T	p.N986N	Chr.12: 89603145-89603145 on Build GRCh38
3955280	c.2869G>C	p.D957H	Chr.12: 89603234-89603234 on Build GRCh38
6869718	c.2874T>G	p.S958R	Chr.12: 89603229-89603229 on Build GRCh38
5587246	c.3001G>A	p.E1001K	Chr.12: 89603102-89603102 on Build GRCh38
4045306	c.2997A>T	p.V999V	Chr.12: 89603106-89603106 on Build GRCh38
3793026	c.3009C>T	p.I1003I	Chr.12: 89603094-89603094 on Build GRCh38
3772747	c.2971C>T	p.R991W	Chr.12: 89603132-89603132 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs780919995	Chr.12: 89603248-89603248 on Build GRCh38
rs779822283	Chr.12: 89603218-89603218 on Build GRCh38
rs771630385	Chr.12: 89603296-89603296 on Build GRCh38
rs370810713	Chr.12: 89603165-89603165 on Build GRCh38
rs11105341	Chr.12: 89603301-89603301 on Build GRCh38
rs377272508	Chr.12: 89603125-89603125 on Build GRCh38
rs778675473	Chr.12: 89603204-89603204 on Build GRCh38
rs376290022	Chr.12: 89603269-89603269 on Build GRCh38
rs756240515	Chr.12: 89603187-89603187 on Build GRCh38
rs1005125190	Chr.12: 89603145-89603145 on Build GRCh38
rs374196525	Chr.12: 89603281-89603281 on Build GRCh38
rs966303879	Chr.12: 89603226-89603226 on Build GRCh38
rs752693675	Chr.12: 89603180-89603180 on Build GRCh38
rs746847972	Chr.12: 89603237-89603237 on Build GRCh38
rs758129782	Chr.12: 89603208-89603208 on Build GRCh38
rs189003061	Chr.12: 89603241-89603241 on Build GRCh38
rs750364043	Chr.12: 89603207-89603207 on Build GRCh38
rs370788275	Chr.12: 89603276-89603276 on Build GRCh38
rs763543000	Chr.12: 89603288-89603288 on Build GRCh38
rs767818173	Chr.12: 89603127-89603127 on Build GRCh38
rs1015210218	Chr.12: 89603196-89603196 on Build GRCh38

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