Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.8: 81660479-81660740 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: IMPA1
Entrez Gene ID: 3612
Gene Name: inositol monophosphatase 1
Gene Aliases: IMP, IMPA
UniGene: Hs.656694
Gene Chromosome Location: Chr.8: 81656916-81686354 on Build GRCh38
Transcripts: NM_001144878.1 NM_001144879.1 NM_005536.3

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
4795026	c.698G>A	p.G233D	Chr.8: 81660536-81660536 on Build GRCh38
4924855	c.632A>G	p.Y211C	Chr.8: 81660602-81660602 on Build GRCh38
4890760	c.627T>G	p.D209E	Chr.8: 81660607-81660607 on Build GRCh38
150500	c.572G>A	p.R191Q	Chr.8: 81660662-81660662 on Build GRCh38
4548842	c.567G>A	p.G189G	Chr.8: 81660667-81660667 on Build GRCh38
4782314	c.749G>A	p.R250Q	Chr.8: 81660662-81660662 on Build GRCh38
751640	c.700G>A	p.V234M	Chr.8: 81660534-81660534 on Build GRCh38
4795025	c.875G>A	p.G292D	Chr.8: 81660536-81660536 on Build GRCh38
4890759	c.804T>G	p.D268E	Chr.8: 81660607-81660607 on Build GRCh38
4924854	c.809A>G	p.Y270C	Chr.8: 81660602-81660602 on Build GRCh38
6343964	c.570C>A	p.I190I	Chr.8: 81660664-81660664 on Build GRCh38
3901766	c.806C>T	p.A269V	Chr.8: 81660605-81660605 on Build GRCh38
6339679	c.674G>C	p.G225A	Chr.8: 81660560-81660560 on Build GRCh38
6685604	c.748C>T	p.R250W	Chr.8: 81660663-81660663 on Build GRCh38
3663901	c.580G>T	p.G194*	Chr.8: 81660654-81660654 on Build GRCh38
3663899	c.581G>T	p.G194V	Chr.8: 81660653-81660653 on Build GRCh38
6685605	c.571C>T	p.R191W	Chr.8: 81660663-81660663 on Build GRCh38
3901767	c.629C>T	p.A210V	Chr.8: 81660605-81660605 on Build GRCh38
1151161	c.877G>A	p.V293M	Chr.8: 81660534-81660534 on Build GRCh38
4548841	c.744G>A	p.G248G	Chr.8: 81660667-81660667 on Build GRCh38
6181931	c.765A>T	p.A255A	Chr.8: 81660646-81660646 on Build GRCh38
245031	c.588A>G	p.A196A	Chr.8: 81660646-81660646 on Build GRCh38
3663898	c.758G>T	p.G253V	Chr.8: 81660653-81660653 on Build GRCh38
3663900	c.757G>T	p.G253*	Chr.8: 81660654-81660654 on Build GRCh38
6343963	c.747C>A	p.I249I	Chr.8: 81660664-81660664 on Build GRCh38
6339678	c.851G>C	p.G284A	Chr.8: 81660560-81660560 on Build GRCh38
6181932	c.588A>T	p.A196A	Chr.8: 81660646-81660646 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs562872543	Chr.8: 81660615-81660615 on Build GRCh38
rs202127208	Chr.8: 81660575-81660575 on Build GRCh38
rs769064564	Chr.8: 81660572-81660572 on Build GRCh38
rs780834689	Chr.8: 81660649-81660649 on Build GRCh38
rs202089380	Chr.8: 81660534-81660534 on Build GRCh38
rs779184992	Chr.8: 81660662-81660662 on Build GRCh38
rs761726155	Chr.8: 81660614-81660614 on Build GRCh38
rs371572810	Chr.8: 81660507-81660507 on Build GRCh38
rs758883028	Chr.8: 81660684-81660684 on Build GRCh38
rs776498442	Chr.8: 81660609-81660609 on Build GRCh38
rs763974663	Chr.8: 81660695-81660695 on Build GRCh38
rs779495553	Chr.8: 81660519-81660519 on Build GRCh38
rs201475007	Chr.8: 81660586-81660586 on Build GRCh38
rs754151177	Chr.8: 81660655-81660655 on Build GRCh38
rs775477038	Chr.8: 81660549-81660549 on Build GRCh38
rs751136547	Chr.8: 81660645-81660645 on Build GRCh38
rs1050474913	Chr.8: 81660535-81660535 on Build GRCh38
rs765899873	Chr.8: 81660634-81660634 on Build GRCh38
rs754560567	Chr.8: 81660646-81660646 on Build GRCh38
rs772816350	Chr.8: 81660506-81660506 on Build GRCh38
rs1009012304	Chr.8: 81660604-81660604 on Build GRCh38
rs200215384	Chr.8: 81660616-81660616 on Build GRCh38
rs775215785	Chr.8: 81660659-81660659 on Build GRCh38
rs778610151	Chr.8: 81660698-81660698 on Build GRCh38
rs200934912	Chr.8: 81660579-81660579 on Build GRCh38
rs762978480	Chr.8: 81660678-81660678 on Build GRCh38
rs149824165	Chr.8: 81660621-81660621 on Build GRCh38
rs760961461	Chr.8: 81660555-81660555 on Build GRCh38
rs780274905	Chr.8: 81660706-81660706 on Build GRCh38
rs200393051	Chr.8: 81660547-81660547 on Build GRCh38

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