Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.20: 41404425-41404698 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: CHD6
Entrez Gene ID: 84181
Gene Name: chromodomain helicase DNA binding protein 6
Gene Aliases: CHD-6, CHD5, RIGB
UniGene: Hs.740645
Gene Chromosome Location: Chr.20: 41402101-41618494 on Build GRCh38
Transcripts: NM_032221.4 XM_005260573.2 XM_005260576.4 XM_011529080.2 XM_011529082.2 XM_017028099.1 XM_017028100.1 XM_017028101.1 XM_017028103.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
4098432	c.8091A>G	p.E2697E	Chr.20: 41404650-41404650 on Build GRCh38
6319241	c.8052C>A	p.N2684K	Chr.20: 41404689-41404689 on Build GRCh38
6159722	c.8138A>T	p.D2713V	Chr.20: 41404603-41404603 on Build GRCh38
5819450	c.8084A>T	p.E2695V	Chr.20: 41404657-41404657 on Build GRCh38
6628105	c.8069C>T	p.A2690V	Chr.20: 41404672-41404672 on Build GRCh38
3291624	c.8066G>A	p.S2689N	Chr.20: 41404675-41404675 on Build GRCh38
3291623	c.8076G>C	p.L2692F	Chr.20: 41404665-41404665 on Build GRCh38
6628122	c.8137G>A	p.D2713N	Chr.20: 41404604-41404604 on Build GRCh38
6628140	c.8090_8091insGA	p.H2698fs*>19	Chr.20: 41404650-41404651 on Build GRCh38
4169332	c.8078C>T	p.P2693L	Chr.20: 41404663-41404663 on Build GRCh38
3291622	c.8079C>T	p.P2693P	Chr.20: 41404662-41404662 on Build GRCh38
4672062	c.8114G>T	p.G2705V	Chr.20: 41404627-41404627 on Build GRCh38
5569639	c.8140A>G	p.T2714A	Chr.20: 41404601-41404601 on Build GRCh38
7224426	c.8063C>T	p.P2688L	Chr.20: 41404678-41404678 on Build GRCh38
1411823	c.8059G>A	p.E2687K	Chr.20: 41404682-41404682 on Build GRCh38
1248219	c.8136C>T	p.N2712N	Chr.20: 41404605-41404605 on Build GRCh38
1411822	c.8148G>T	p.*2716Y	Chr.20: 41404593-41404593 on Build GRCh38
4440740	c.8064C>T	p.P2688P	Chr.20: 41404677-41404677 on Build GRCh38
5857878	c.8071C>T	p.P2691S	Chr.20: 41404670-41404670 on Build GRCh38
1681677	c.8112G>T	p.E2704D	Chr.20: 41404629-41404629 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs774422854	Chr.20: 41404586-41404586 on Build GRCh38
rs758136461	Chr.20: 41404629-41404629 on Build GRCh38
rs34155666	Chr.20: 41404634-41404635 on Build GRCh38
rs567803054	Chr.20: 41404492-41404492 on Build GRCh38
rs373801105	Chr.20: 41404661-41404661 on Build GRCh38
rs766392150	Chr.20: 41404575-41404575 on Build GRCh38
rs767933950	Chr.20: 41404602-41404602 on Build GRCh38
rs774367979	Chr.20: 41404676-41404676 on Build GRCh38
rs80216136	Chr.20: 41404479-41404479 on Build GRCh38
rs376824126	Chr.20: 41404560-41404560 on Build GRCh38
rs373499260	Chr.20: 41404639-41404639 on Build GRCh38
rs199910662	Chr.20: 41404544-41404544 on Build GRCh38
rs750030866	Chr.20: 41404627-41404627 on Build GRCh38
rs769676749	Chr.20: 41404563-41404563 on Build GRCh38
rs759999480	Chr.20: 41404596-41404596 on Build GRCh38
rs756404610	Chr.20: 41404614-41404614 on Build GRCh38
rs763222701	Chr.20: 41404568-41404568 on Build GRCh38
rs370635651	Chr.20: 41404618-41404618 on Build GRCh38
rs148480354	Chr.20: 41404605-41404605 on Build GRCh38
rs370586122	Chr.20: 41404665-41404665 on Build GRCh38
rs942534680	Chr.20: 41404499-41404499 on Build GRCh38
rs780966446	Chr.20: 41404646-41404646 on Build GRCh38
rs746546629	Chr.20: 41404634-41404634 on Build GRCh38
rs570357924	Chr.20: 41404638-41404638 on Build GRCh38
rs539457727	Chr.20: 41404643-41404643 on Build GRCh38
rs1047269026	Chr.20: 41404604-41404604 on Build GRCh38
rs1011993826	Chr.20: 41404491-41404491 on Build GRCh38
rs376331754	Chr.20: 41404652-41404652 on Build GRCh38
rs1039534619	Chr.20: 41404511-41404511 on Build GRCh38
rs1023429103	Chr.20: 41404493-41404493 on Build GRCh38
rs749448664	Chr.20: 41404662-41404662 on Build GRCh38
rs971318809	Chr.20: 41404664-41404664 on Build GRCh38
rs200359247	Chr.20: 41404655-41404655 on Build GRCh38
rs994715989	Chr.20: 41404453-41404453 on Build GRCh38
rs779638279	Chr.20: 41404633-41404633 on Build GRCh38

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