Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.9: 137914617-137914870 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: CACNA1B
Entrez Gene ID: 774
Gene Name: calcium voltage-gated channel subunit alpha1 B
Gene Aliases: BIII, CACNL1A5, CACNN, Cav2.2, DYT23
UniGene: Hs.495522
Gene Chromosome Location: Chr.9: 137877789-138124624 on Build GRCh38
Transcripts: NM_000718.3 NM_001243812.1 XM_011518991.2 XM_011518992.2 XM_011518993.2 XM_011518994.2 XM_017015115.1 XM_017015116.1 XM_017015117.1 XM_017015118.1 XM_017015119.1 XM_017015120.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
6115309	c.634G>T	p.V212L	Chr.9: 137914665-137914665 on Build GRCh38
7303474	c.655G>T	p.A219S	Chr.9: 137914686-137914686 on Build GRCh38
753007	c.717C>T	p.I239I	Chr.9: 137914748-137914748 on Build GRCh38
4393766	c.729G>A	p.E243E	Chr.9: 137914760-137914760 on Build GRCh38
7196996	c.713C>A	p.A238D	Chr.9: 137914744-137914744 on Build GRCh38
7147908	c.775G>T	p.D259Y	Chr.9: 137914806-137914806 on Build GRCh38
4504635	c.670C>T	p.L224L	Chr.9: 137914701-137914701 on Build GRCh38
5711247	c.691T>G	p.F231V	Chr.9: 137914722-137914722 on Build GRCh38
3375190	c.655G>A	p.A219T	Chr.9: 137914686-137914686 on Build GRCh38
3906196	c.712G>A	p.A238T	Chr.9: 137914743-137914743 on Build GRCh38
7303475	c.655G>T	p.A219S	Chr.9: 137914686-137914686 on Build GRCh38
1247085	c.724C>T	p.L242L	Chr.9: 137914755-137914755 on Build GRCh38
6115310	c.634G>T	p.V212L	Chr.9: 137914665-137914665 on Build GRCh38
3089811	c.767A>G	p.N256S	Chr.9: 137914798-137914798 on Build GRCh38
4518420	c.644_645CC>TT	p.S215F	Chr.9: 137914675-137914676 on Build GRCh38
7147907	c.775G>T	p.D259Y	Chr.9: 137914806-137914806 on Build GRCh38
3656108	c.738G>A	p.M246I	Chr.9: 137914769-137914769 on Build GRCh38
3656106	c.664C>T	p.P222S	Chr.9: 137914695-137914695 on Build GRCh38
7196997	c.713C>A	p.A238D	Chr.9: 137914744-137914744 on Build GRCh38
5711246	c.691T>G	p.F231V	Chr.9: 137914722-137914722 on Build GRCh38
3656107	c.665C>T	p.P222L	Chr.9: 137914696-137914696 on Build GRCh38
5423345	c.738delG	p.G247fs*59	Chr.9: 137914769-137914769 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs200521478	Chr.9: 137914839-137914839 on Build GRCh38
rs773179550	Chr.9: 137914736-137914736 on Build GRCh38
rs199792680	Chr.9: 137914834-137914834 on Build GRCh38
rs763939363	Chr.9: 137914771-137914771 on Build GRCh38
rs769630341	Chr.9: 137914680-137914680 on Build GRCh38
rs751021410	Chr.9: 137914650-137914650 on Build GRCh38
rs761312939	Chr.9: 137914835-137914835 on Build GRCh38
rs372939958	Chr.9: 137914641-137914641 on Build GRCh38
rs760088580	Chr.9: 137914815-137914815 on Build GRCh38
rs11137301	Chr.9: 137914847-137914847 on Build GRCh38
rs757142084	Chr.9: 137914667-137914667 on Build GRCh38
rs200274455	Chr.9: 137914746-137914746 on Build GRCh38
rs779795778	Chr.9: 137914693-137914693 on Build GRCh38
rs997663132	Chr.9: 137914777-137914777 on Build GRCh38
rs760741224	Chr.9: 137914739-137914739 on Build GRCh38
rs532639291	Chr.9: 137914846-137914846 on Build GRCh38
rs781168541	Chr.9: 137914670-137914670 on Build GRCh38
rs150072064	Chr.9: 137914816-137914816 on Build GRCh38
rs567155794	Chr.9: 137914819-137914819 on Build GRCh38
rs1039293406	Chr.9: 137914643-137914643 on Build GRCh38
rs201810627	Chr.9: 137914708-137914708 on Build GRCh38
rs772290130	Chr.9: 137914733-137914733 on Build GRCh38
rs777326436	Chr.9: 137914799-137914799 on Build GRCh38
rs958126621	Chr.9: 137914823-137914823 on Build GRCh38
rs748352783	Chr.9: 137914715-137914715 on Build GRCh38
rs762523004	Chr.9: 137914820-137914820 on Build GRCh38
rs745795777	Chr.9: 137914679-137914679 on Build GRCh38
rs771131603	Chr.9: 137914785-137914785 on Build GRCh38

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