Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.7: 6028544-6028773 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: EIF2AK1
Entrez Gene ID: 27102
Gene Name: eukaryotic translation initiation factor 2 alpha kinase 1
Gene Aliases: HCR, HRI
UniGene: Hs.520205
Gene Chromosome Location: Chr.7: 6022247-6059229 on Build GRCh38
Transcripts: NM_001134335.1 NM_014413.3

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
3950672	c.1498G>C	p.E500Q	Chr.7: 6028647-6028647 on Build GRCh38
5039075	c.1511G>T	p.G504V	Chr.7: 6028634-6028634 on Build GRCh38
4409336	c.1091C>A	p.T364K	Chr.7: 6028682-6028682 on Build GRCh38
6448027	c.1091C>T	p.T364M	Chr.7: 6028682-6028682 on Build GRCh38
5038619	c.1141delT	p.S381fs*17	Chr.7: 6028632-6028632 on Build GRCh38
310830	c.1448-1G>A	p.?	Chr.7: 6028698-6028698 on Build GRCh38
7235525	c.1126G>A	p.E376K	Chr.7: 6028647-6028647 on Build GRCh38
5038618	c.1513delT	p.S505fs*17	Chr.7: 6028632-6028632 on Build GRCh38
3942269	c.1462A>G	p.T488A	Chr.7: 6028683-6028683 on Build GRCh38
7235524	c.1498G>A	p.E500K	Chr.7: 6028647-6028647 on Build GRCh38
5039076	c.1139G>T	p.G380V	Chr.7: 6028634-6028634 on Build GRCh38
4609338	c.1126G>T	p.E376*	Chr.7: 6028647-6028647 on Build GRCh38
342020	c.1514C>G	p.S505C	Chr.7: 6028631-6028631 on Build GRCh38
6448026	c.1463C>T	p.T488M	Chr.7: 6028682-6028682 on Build GRCh38
4409335	c.1463C>A	p.T488K	Chr.7: 6028682-6028682 on Build GRCh38
5746683	c.1147T>C	p.Y383H	Chr.7: 6028626-6028626 on Build GRCh38
5746682	c.1519T>C	p.Y507H	Chr.7: 6028626-6028626 on Build GRCh38
3950673	c.1126G>C	p.E376Q	Chr.7: 6028647-6028647 on Build GRCh38
4609337	c.1498G>T	p.E500*	Chr.7: 6028647-6028647 on Build GRCh38
3942270	c.1090A>G	p.T364A	Chr.7: 6028683-6028683 on Build GRCh38
6652619	c.1101G>A	p.V367V	Chr.7: 6028672-6028672 on Build GRCh38
1238765	c.1486T>C	p.Y496H	Chr.7: 6028659-6028659 on Build GRCh38
4834268	c.1469G>C	p.R490T	Chr.7: 6028676-6028676 on Build GRCh38
6652618	c.1473G>A	p.V491V	Chr.7: 6028672-6028672 on Build GRCh38
4834269	c.1097G>C	p.R366T	Chr.7: 6028676-6028676 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs376152082	Chr.7: 6028697-6028697 on Build GRCh38
rs371787803	Chr.7: 6028601-6028601 on Build GRCh38
rs769682382	Chr.7: 6028682-6028682 on Build GRCh38
rs144797860	Chr.7: 6028667-6028667 on Build GRCh38
rs756875216	Chr.7: 6028655-6028655 on Build GRCh38
rs768572436	Chr.7: 6028572-6028572 on Build GRCh38
rs532345337	Chr.7: 6028648-6028648 on Build GRCh38
rs770215808	Chr.7: 6028627-6028627 on Build GRCh38
rs759847990	Chr.7: 6028625-6028625 on Build GRCh38
rs746043505	Chr.7: 6028714-6028714 on Build GRCh38
rs368661636	Chr.7: 6028660-6028660 on Build GRCh38
rs771105947	Chr.7: 6028592-6028592 on Build GRCh38
rs747076833	Chr.7: 6028587-6028587 on Build GRCh38
rs947583310	Chr.7: 6028647-6028647 on Build GRCh38
rs763388999	Chr.7: 6028737-6028737 on Build GRCh38
rs138548924	Chr.7: 6028651-6028651 on Build GRCh38
rs182474233	Chr.7: 6028705-6028705 on Build GRCh38
rs372082679	Chr.7: 6028703-6028703 on Build GRCh38
rs777899865	Chr.7: 6028581-6028581 on Build GRCh38
rs748149087	Chr.7: 6028676-6028676 on Build GRCh38
rs149262605	Chr.7: 6028657-6028657 on Build GRCh38
rs566395713	Chr.7: 6028635-6028635 on Build GRCh38
rs1007954194	Chr.7: 6028662-6028662 on Build GRCh38
rs776153903	Chr.7: 6028629-6028629 on Build GRCh38
rs779885923	Chr.7: 6028681-6028681 on Build GRCh38
rs370810725	Chr.7: 6028689-6028689 on Build GRCh38
rs754913840	Chr.7: 6028690-6028691 on Build GRCh38
rs982629359	Chr.7: 6028731-6028731 on Build GRCh38
rs755878275	Chr.7: 6028677-6028677 on Build GRCh38
rs776063827	Chr.7: 6028727-6028727 on Build GRCh38
rs138441452	Chr.7: 6028685-6028685 on Build GRCh38
rs747079321	Chr.7: 6028702-6028702 on Build GRCh38
rs751164433	Chr.7: 6028656-6028656 on Build GRCh38
rs753685999	Chr.7: 6028595-6028596 on Build GRCh38

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