Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.12: 30710309-30710550 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: CAPRIN2
Entrez Gene ID: 65981
Gene Name: caprin family member 2
Gene Aliases: C1QDC1, EEG-1, EEG1, RNG140
UniGene: Hs.234355
Gene Chromosome Location: Chr.12: 30709552-30754994 on Build GRCh38
Transcripts: NM_001002259.2 NM_001206856.2 NM_001319842.1 NM_001319843.1 NM_001319844.1 NM_001319845.1 NM_001319846.1 NM_023925.4 NM_032156.4 XM_006719138.3 XM_006719139.3 XM_006719140.3 XM_006719142.3 XM_006719144.3 XM_006719145.3 XM_006719146.3 XM_006719147.3 XM_017019851.1 XM_017019852.1 XM_017019853.1 XM_017019854.1 XM_017019855.1 XM_017019856.1 XM_017019857.1 XM_017019858.1 XM_017019859.1 XM_017019860.1 XM_017019861.1 XM_017019862.1 XM_017019863.1 XM_017019864.1 XM_017019865.1 XM_017019866.1 XM_017019867.1 XM_017019868.1 XM_017019869.1 XM_017019870.1 XM_017019871.1 XM_017019872.1 XM_017019873.1 XM_017019874.1 XM_017019875.1 XM_017019876.1 XM_017019877.1 XM_017019878.1 XM_017019879.1 XM_017019880.1 XM_017019881.1 XM_017019882.1 XM_017019883.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
2205129	c.2903G>A	p.R968H	Chr.12: 30710383-30710383 on Build GRCh38
7277097	c.2878A>G	p.R960G	Chr.12: 30710449-30710449 on Build GRCh38
6620007	c.2905A>G	p.S969G	Chr.12: 30710381-30710381 on Build GRCh38
5696414	c.2955G>T	p.L985L	Chr.12: 30710331-30710331 on Build GRCh38
6620001	c.2959G>A	p.V987I	Chr.12: 30710327-30710327 on Build GRCh38
4777589	c.2897A>C	p.D966A	Chr.12: 30710389-30710389 on Build GRCh38
5693351	c.2850A>G	p.P950P	Chr.12: 30710436-30710436 on Build GRCh38
3460085	c.2915C>T	p.P972L	Chr.12: 30710371-30710371 on Build GRCh38
5346157	c.2905A>T	p.S969C	Chr.12: 30710381-30710381 on Build GRCh38
5949547	c.2953C>T	p.L985L	Chr.12: 30710333-30710333 on Build GRCh38
6451263	c.2814T>C	p.A938A	Chr.12: 30710513-30710513 on Build GRCh38
4926328	c.2912C>T	p.T971I	Chr.12: 30710374-30710374 on Build GRCh38
5434860	c.2881T>C	p.*961R	Chr.12: 30710446-30710446 on Build GRCh38
1361180	c.2855delG	p.R952fs*19	Chr.12: 30710431-30710431 on Build GRCh38
4849937	c.2943A>T	p.A981A	Chr.12: 30710343-30710343 on Build GRCh38
6894731	c.2834C>T	p.S945F	Chr.12: 30710452-30710452 on Build GRCh38
5832034	c.2862T>G	p.G954G	Chr.12: 30710465-30710465 on Build GRCh38
4669197	c.2944G>A	p.A982T	Chr.12: 30710342-30710342 on Build GRCh38
5434859	c.2840T>C	p.V947A	Chr.12: 30710446-30710446 on Build GRCh38
386516	c.2823G>C	p.W941C	Chr.12: 30710463-30710463 on Build GRCh38
7122598	c.2902C>A	p.R968S	Chr.12: 30710384-30710384 on Build GRCh38
3811834	c.2821T>G	p.W941G	Chr.12: 30710465-30710465 on Build GRCh38
6894732	c.2875C>T	p.L959F	Chr.12: 30710452-30710452 on Build GRCh38
243477	c.2939C>G	p.P980R	Chr.12: 30710347-30710347 on Build GRCh38
3792517	c.2878G>T	p.G960C	Chr.12: 30710408-30710408 on Build GRCh38
938647	c.2863G>A	p.E955K	Chr.12: 30710423-30710423 on Build GRCh38
7277098	c.2837A>G	p.Q946R	Chr.12: 30710449-30710449 on Build GRCh38
6619987	c.2966T>C	p.V989A	Chr.12: 30710320-30710320 on Build GRCh38
7227440	c.2938C>T	p.P980S	Chr.12: 30710348-30710348 on Build GRCh38
5580520	c.2922T>C	p.D974D	Chr.12: 30710364-30710364 on Build GRCh38
1660979	c.2845A>T	p.S949C	Chr.12: 30710441-30710441 on Build GRCh38
6136828	c.2904T>A	p.R968R	Chr.12: 30710382-30710382 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs747195058	Chr.12: 30710498-30710498 on Build GRCh38
rs201095477	Chr.12: 30710412-30710412 on Build GRCh38
rs372208056	Chr.12: 30710337-30710337 on Build GRCh38
rs79552778	Chr.12: 30710379-30710379 on Build GRCh38
rs761381989	Chr.12: 30710432-30710432 on Build GRCh38
rs973720071	Chr.12: 30710470-30710470 on Build GRCh38
rs965803693	Chr.12: 30710331-30710331 on Build GRCh38
rs767335762	Chr.12: 30710433-30710433 on Build GRCh38
rs756585609	Chr.12: 30710446-30710446 on Build GRCh38
rs927003563	Chr.12: 30710409-30710409 on Build GRCh38
rs140741615	Chr.12: 30710336-30710336 on Build GRCh38
rs772253137	Chr.12: 30710383-30710383 on Build GRCh38
rs375234262	Chr.12: 30710361-30710361 on Build GRCh38
rs371328465	Chr.12: 30710424-30710424 on Build GRCh38
rs750076759	Chr.12: 30710445-30710445 on Build GRCh38
rs878879989	Chr.12: 30710357-30710357 on Build GRCh38
rs535610393	Chr.12: 30710346-30710346 on Build GRCh38
rs759274017	Chr.12: 30710393-30710393 on Build GRCh38
rs775209566	Chr.12: 30710499-30710499 on Build GRCh38
rs755379630	Chr.12: 30710455-30710455 on Build GRCh38
rs780659467	Chr.12: 30710340-30710340 on Build GRCh38
rs367800608	Chr.12: 30710384-30710384 on Build GRCh38
rs762953715	Chr.12: 30710520-30710520 on Build GRCh38
rs200624700	Chr.12: 30710486-30710486 on Build GRCh38
rs754416397	Chr.12: 30710451-30710451 on Build GRCh38
rs775373364	Chr.12: 30710411-30710411 on Build GRCh38
rs761265039	Chr.12: 30710513-30710513 on Build GRCh38
rs769605672	Chr.12: 30710406-30710406 on Build GRCh38
rs976348698	Chr.12: 30710347-30710347 on Build GRCh38
rs763676110	Chr.12: 30710423-30710423 on Build GRCh38
rs1044833	Chr.12: 30710471-30710471 on Build GRCh38
rs772173740	Chr.12: 30710490-30710490 on Build GRCh38
rs779052048	Chr.12: 30710472-30710472 on Build GRCh38
rs780524389	Chr.12: 30710447-30710447 on Build GRCh38
rs778912498	Chr.12: 30710378-30710378 on Build GRCh38
rs778012995	Chr.12: 30710497-30710497 on Build GRCh38

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