Product Details

Primer Sequences

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Primer Chromosome Location

Chr.12: 42387439-42387668 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

PPHLN1

Entrez Gene ID

51535

Gene Name

periphilin 1

Gene Aliases

CR, HSPC206, HSPC232

UniGene

Hs.444157

Gene Chromosome Location

Chr.12: 42326126-42448621 on Build GRCh38

Transcripts

NM_001143787.1 NM_001143788.1 NM_001143789.1 NM_016488.6 NM_201438.1 NM_201439.1 NM_201440.1 NM_201515.1 XM_005268962.3 XM_011538459.2 XM_011538465.2 XM_011538467.2 XM_011538470.2 XM_011538471.2 XM_017019434.1 XM_017019435.1 XM_017019436.1 XM_017019437.1 XM_017019438.1 XM_017019439.1 XM_017019440.1 XM_017019441.1 XM_017019442.1 XM_017019443.1 XM_017019444.1 XM_017019445.1 XM_017019446.1 XM_017019447.1 XM_017019448.1 XM_017019449.1 XM_017019450.1 XM_017019451.1 XM_017019452.1 XM_017019453.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6753424	c.608A>T	p.D203V	Chr.12: 42387495-42387495 on Build GRCh38
6753422	c.443A>T	p.D148V	Chr.12: 42387495-42387495 on Build GRCh38
6258242	c.460G>T	p.G154C	Chr.12: 42387512-42387512 on Build GRCh38
3384344	c.644C>G	p.S215*	Chr.12: 42387531-42387531 on Build GRCh38
6258243	c.646G>T	p.G216C	Chr.12: 42387512-42387512 on Build GRCh38
3723159	c.598A>G	p.T200A	Chr.12: 42387485-42387485 on Build GRCh38
5201004	c.473C>A	p.S158Y	Chr.12: 42387525-42387525 on Build GRCh38
6395153	c.575A>G	p.E192G	Chr.12: 42387462-42387462 on Build GRCh38
3723158	c.619A>G	p.T207A	Chr.12: 42387485-42387485 on Build GRCh38
3723157	c.433A>G	p.T145A	Chr.12: 42387485-42387485 on Build GRCh38
6753423	c.629A>T	p.D210V	Chr.12: 42387495-42387495 on Build GRCh38
6395154	c.410A>G	p.E137G	Chr.12: 42387462-42387462 on Build GRCh38
6395155	c.596A>G	p.E199G	Chr.12: 42387462-42387462 on Build GRCh38
6395156	c.575A>G	p.E192G	Chr.12: 42387462-42387462 on Build GRCh38
3723156	c.598A>G	p.T200A	Chr.12: 42387485-42387485 on Build GRCh38
3384346	c.665C>G	p.S222*	Chr.12: 42387531-42387531 on Build GRCh38
3384345	c.479C>G	p.S160*	Chr.12: 42387531-42387531 on Build GRCh38
6753421	c.608A>T	p.D203V	Chr.12: 42387495-42387495 on Build GRCh38
6258241	c.625G>T	p.G209C	Chr.12: 42387512-42387512 on Build GRCh38
431087	c.638C>A	p.S213Y	Chr.12: 42387525-42387525 on Build GRCh38
1133957	c.659C>A	p.S220Y	Chr.12: 42387525-42387525 on Build GRCh38
3384347	c.644C>G	p.S215*	Chr.12: 42387531-42387531 on Build GRCh38
431088	c.638C>A	p.S213Y	Chr.12: 42387525-42387525 on Build GRCh38
6258244	c.625G>T	p.G209C	Chr.12: 42387512-42387512 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs764138164	Chr.12: 42387586-42387586 on Build GRCh38
rs374534618	Chr.12: 42387485-42387485 on Build GRCh38
rs749793965	Chr.12: 42387502-42387502 on Build GRCh38
rs769247769	Chr.12: 42387503-42387503 on Build GRCh38
rs779125538	Chr.12: 42387508-42387508 on Build GRCh38
rs556118803	Chr.12: 42387518-42387518 on Build GRCh38
rs773500450	Chr.12: 42387524-42387524 on Build GRCh38
rs774173455	Chr.12: 42387587-42387587 on Build GRCh38
rs368593861	Chr.12: 42387574-42387574 on Build GRCh38
rs1015113520	Chr.12: 42387578-42387578 on Build GRCh38
rs937647657	Chr.12: 42387494-42387494 on Build GRCh38
rs771119579	Chr.12: 42387556-42387556 on Build GRCh38
rs141145173	Chr.12: 42387585-42387585 on Build GRCh38
rs776915694	Chr.12: 42387558-42387558 on Build GRCh38
rs755552152	Chr.12: 42387492-42387492 on Build GRCh38
rs779089561	Chr.12: 42387563-42387565 on Build GRCh38
rs779603127	Chr.12: 42387493-42387493 on Build GRCh38
rs747247433	Chr.12: 42387540-42387540 on Build GRCh38

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