Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.12: 7483460-7483713 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: CD163
Entrez Gene ID: 9332
Gene Name: CD163 molecule
Gene Aliases: M130, MM130, SCARI1
UniGene: Hs.504641
Gene Chromosome Location: Chr.12: 7470816-7503818 on Build GRCh38
Transcripts: NM_004244.5 NM_203416.3 XM_005253528.4 XM_005253529.4 XM_017020231.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
4540191	c.2801G>A	p.G934E	Chr.12: 7483654-7483654 on Build GRCh38
3872519	c.2941G>A	p.E981K	Chr.12: 7483514-7483514 on Build GRCh38
6073554	c.2839G>T	p.G947*	Chr.12: 7483616-7483616 on Build GRCh38
7195867	c.2909T>G	p.L970R	Chr.12: 7483546-7483546 on Build GRCh38
7195868	c.3008T>G	p.L1003R	Chr.12: 7483546-7483546 on Build GRCh38
4670342	c.2978T>G	p.L993R	Chr.12: 7483477-7483477 on Build GRCh38
4540192	c.2900G>A	p.G967E	Chr.12: 7483654-7483654 on Build GRCh38
4395770	c.2970G>A	p.P990P	Chr.12: 7483485-7483485 on Build GRCh38
5568990	c.2869T>C	p.S957P	Chr.12: 7483586-7483586 on Build GRCh38
5841907	c.2846C>T	p.S949F	Chr.12: 7483609-7483609 on Build GRCh38
4809984	c.2986G>T	p.A996S	Chr.12: 7483568-7483568 on Build GRCh38
7414882	c.2926G>T	p.E976*	Chr.12: 7483628-7483628 on Build GRCh38
6073555	c.2938G>T	p.G980*	Chr.12: 7483616-7483616 on Build GRCh38
5520807	c.2992G>A	p.V998M	Chr.12: 7483562-7483562 on Build GRCh38
3955153	c.2853G>T	p.G951G	Chr.12: 7483602-7483602 on Build GRCh38
4975290	c.3027G>A	p.L1009L	Chr.12: 7483527-7483527 on Build GRCh38
5841908	c.2945C>T	p.S982F	Chr.12: 7483609-7483609 on Build GRCh38
4898783	c.2892G>A	p.Q964Q	Chr.12: 7483563-7483563 on Build GRCh38
4864422	c.3019C>T	p.P1007S	Chr.12: 7483535-7483535 on Build GRCh38
6274430	c.2880C>A	p.N960K	Chr.12: 7483674-7483674 on Build GRCh38
4540646	c.2875G>A	p.D959N	Chr.12: 7483580-7483580 on Build GRCh38
159850	c.2887G>T	p.A963S	Chr.12: 7483568-7483568 on Build GRCh38
7203497	c.2940A>T	p.G980G	Chr.12: 7483614-7483614 on Build GRCh38
7203496	c.2841A>T	p.G947G	Chr.12: 7483614-7483614 on Build GRCh38
6073556	c.2959_2960GG>TT	p.G987L	Chr.12: 7483495-7483496 on Build GRCh38
5520806	c.2893G>A	p.V965M	Chr.12: 7483562-7483562 on Build GRCh38
4540647	c.2974G>A	p.D992N	Chr.12: 7483580-7483580 on Build GRCh38
1645712	c.3069G>C	p.P1023P	Chr.12: 7483485-7483485 on Build GRCh38
4975289	c.2928G>A	p.L976L	Chr.12: 7483527-7483527 on Build GRCh38
5669541	c.2999G>T	p.C1000F	Chr.12: 7483555-7483555 on Build GRCh38
5376018	c.3059G>A	p.G1020E	Chr.12: 7483495-7483495 on Build GRCh38
5669540	c.2900G>T	p.C967F	Chr.12: 7483555-7483555 on Build GRCh38
7414881	c.2827G>T	p.E943*	Chr.12: 7483628-7483628 on Build GRCh38
4670343	c.3077T>G	p.L1026R	Chr.12: 7483477-7483477 on Build GRCh38
6073557	c.3058_3059GG>TT	p.G1020L	Chr.12: 7483495-7483496 on Build GRCh38
4400798	c.2983G>A	p.D995N	Chr.12: 7483571-7483571 on Build GRCh38
5376017	c.2960G>A	p.G987E	Chr.12: 7483495-7483495 on Build GRCh38
4898784	c.2991G>A	p.Q997Q	Chr.12: 7483563-7483563 on Build GRCh38
695050	c.2834G>A	p.W945*	Chr.12: 7483621-7483621 on Build GRCh38
3872520	c.3040G>A	p.E1014K	Chr.12: 7483514-7483514 on Build GRCh38
4400797	c.2884G>A	p.D962N	Chr.12: 7483571-7483571 on Build GRCh38
3465387	c.2811C>T	p.S937S	Chr.12: 7483644-7483644 on Build GRCh38
6274429	c.2781C>A	p.N927K	Chr.12: 7483674-7483674 on Build GRCh38
4395771	c.3069G>A	p.P1023P	Chr.12: 7483485-7483485 on Build GRCh38
5568991	c.2968T>C	p.S990P	Chr.12: 7483586-7483586 on Build GRCh38
3465388	c.2910C>T	p.S970S	Chr.12: 7483644-7483644 on Build GRCh38
2102574	c.3051T>C	p.F1017F	Chr.12: 7483503-7483503 on Build GRCh38
2102573	c.2952T>C	p.F984F	Chr.12: 7483503-7483503 on Build GRCh38
4860813	c.2933G>A	p.W978*	Chr.12: 7483621-7483621 on Build GRCh38
7162443	c.2983G>A	p.E995K	Chr.12: 7483472-7483472 on Build GRCh38
7162444	c.3082G>A	p.E1028K	Chr.12: 7483472-7483472 on Build GRCh38
468906	c.2970G>C	p.P990P	Chr.12: 7483485-7483485 on Build GRCh38
943503	c.2920C>T	p.P974S	Chr.12: 7483535-7483535 on Build GRCh38
3955154	c.2952G>T	p.G984G	Chr.12: 7483602-7483602 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs768204023	Chr.12: 7483486-7483486 on Build GRCh38
rs776402823	Chr.12: 7483494-7483494 on Build GRCh38
rs1045655047	Chr.12: 7483488-7483488 on Build GRCh38
rs775082662	Chr.12: 7483485-7483485 on Build GRCh38
rs757152352	Chr.12: 7483617-7483617 on Build GRCh38
rs750247723	Chr.12: 7483625-7483625 on Build GRCh38
rs371406699	Chr.12: 7483572-7483572 on Build GRCh38
rs753885158	Chr.12: 7483613-7483613 on Build GRCh38
rs763870982	Chr.12: 7483571-7483571 on Build GRCh38
rs764142833	Chr.12: 7483574-7483574 on Build GRCh38
rs776200093	Chr.12: 7483499-7483499 on Build GRCh38
rs199560015	Chr.12: 7483641-7483641 on Build GRCh38
rs771413158	Chr.12: 7483518-7483518 on Build GRCh38
rs780582176	Chr.12: 7483669-7483669 on Build GRCh38
rs763374425	Chr.12: 7483511-7483511 on Build GRCh38
rs746721451	Chr.12: 7483635-7483635 on Build GRCh38
rs761565641	Chr.12: 7483626-7483626 on Build GRCh38
rs372790972	Chr.12: 7483557-7483557 on Build GRCh38
rs774603375	Chr.12: 7483527-7483527 on Build GRCh38
rs141756075	Chr.12: 7483564-7483564 on Build GRCh38
rs753020548	Chr.12: 7483563-7483563 on Build GRCh38
rs767965678	Chr.12: 7483548-7483548 on Build GRCh38
rs759943157	Chr.12: 7483531-7483531 on Build GRCh38
rs779801921	Chr.12: 7483631-7483631 on Build GRCh38
rs745473362	Chr.12: 7483618-7483618 on Build GRCh38
rs368897599	Chr.12: 7483566-7483566 on Build GRCh38
rs147938240	Chr.12: 7483675-7483675 on Build GRCh38
rs964444440	Chr.12: 7483634-7483634 on Build GRCh38

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