Product Details

Primer Sequences

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Primer Chromosome Location

Chr.4: 41748346-41748517 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

PHOX2B

Entrez Gene ID

8929

Gene Name

paired like homeobox 2b

Gene Aliases

NBLST2, NBPhox, PMX2B

UniGene

Hs.87202

Gene Chromosome Location

Chr.4: 41744082-41748970 on Build GRCh38

Transcripts

NM_003924.3

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
3603898	c.132T>A	p.Y44*	Chr.4: 41748479-41748479 on Build GRCh38
5884023	c.119G>A	p.S40N	Chr.4: 41748492-41748492 on Build GRCh38
262923	c.206C>A	p.T69N	Chr.4: 41748405-41748405 on Build GRCh38
6983890	c.166G>A	p.G56S	Chr.4: 41748445-41748445 on Build GRCh38
3603897	c.177C>T	p.S59S	Chr.4: 41748434-41748434 on Build GRCh38
6917099	c.157G>T	p.A53S	Chr.4: 41748454-41748454 on Build GRCh38
3603896	c.213G>A	p.R71R	Chr.4: 41748398-41748398 on Build GRCh38
6915310	c.106_107insT	p.C36fs*10	Chr.4: 41748504-41748505 on Build GRCh38
6974533	c.214G>A	p.D72N	Chr.4: 41748397-41748397 on Build GRCh38
5694290	c.165C>G	p.S55S	Chr.4: 41748446-41748446 on Build GRCh38
1670969	c.187G>T	p.G63*	Chr.4: 41748424-41748424 on Build GRCh38
4565022	c.164_165CC>TT	p.S55F	Chr.4: 41748446-41748447 on Build GRCh38
3946357	c.135C>A	p.N45K	Chr.4: 41748476-41748476 on Build GRCh38
6277684	c.184C>T	p.P62S	Chr.4: 41748427-41748427 on Build GRCh38
6226202	c.165C>T	p.S55S	Chr.4: 41748446-41748446 on Build GRCh38
4971464	c.158C>T	p.A53V	Chr.4: 41748453-41748453 on Build GRCh38
6929610	c.208delC	p.L70fs*64	Chr.4: 41748403-41748403 on Build GRCh38
6100482	c.156G>T	p.G52G	Chr.4: 41748455-41748455 on Build GRCh38
6986488	c.227G>C	p.S76T	Chr.4: 41748384-41748384 on Build GRCh38
6922400	c.191C>T	p.S64F	Chr.4: 41748420-41748420 on Build GRCh38
6100481	c.137C>A	p.P46Q	Chr.4: 41748474-41748474 on Build GRCh38
5893005	c.220C>T	p.Q74*	Chr.4: 41748391-41748391 on Build GRCh38
6986245	c.198C>A	p.S66R	Chr.4: 41748413-41748413 on Build GRCh38
6922146	c.178C>G	p.L60V	Chr.4: 41748433-41748433 on Build GRCh38
2847590	c.174T>G	p.P58P	Chr.4: 41748437-41748437 on Build GRCh38
2847587	c.230C>T	p.P77L	Chr.4: 41748381-41748381 on Build GRCh38
7343364	c.229_230CC>TT	p.P77L	Chr.4: 41748381-41748382 on Build GRCh38
1055423	c.126C>A	p.F42L	Chr.4: 41748485-41748485 on Build GRCh38
733457	c.223A>T	p.S75C	Chr.4: 41748388-41748388 on Build GRCh38
6938778	c.146C>A	p.T49N	Chr.4: 41748465-41748465 on Build GRCh38
733456	c.168C>A	p.G56G	Chr.4: 41748443-41748443 on Build GRCh38
1670968	c.188G>A	p.G63E	Chr.4: 41748423-41748423 on Build GRCh38
4528739	c.155G>A	p.G52E	Chr.4: 41748456-41748456 on Build GRCh38
6745582	c.238G>A	p.A80T	Chr.4: 41748373-41748373 on Build GRCh38
1644890	c.188G>T	p.G63V	Chr.4: 41748423-41748423 on Build GRCh38
357002	c.104C>T	p.S35F	Chr.4: 41748507-41748507 on Build GRCh38
5537010	c.176C>T	p.S59F	Chr.4: 41748435-41748435 on Build GRCh38
1429725	c.234C>T	p.Y78Y	Chr.4: 41748377-41748377 on Build GRCh38
4159075	c.100A>G	p.S34G	Chr.4: 41748511-41748511 on Build GRCh38
2847591	c.168C>T	p.G56G	Chr.4: 41748443-41748443 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs756519209	Chr.4: 41748491-41748491 on Build GRCh38
rs763699416	Chr.4: 41748425-41748425 on Build GRCh38
rs73810366	Chr.4: 41748377-41748377 on Build GRCh38
rs376060053	Chr.4: 41748380-41748380 on Build GRCh38
rs550472167	Chr.4: 41748373-41748373 on Build GRCh38
rs946362319	Chr.4: 41748429-41748429 on Build GRCh38
rs766500239	Chr.4: 41748497-41748497 on Build GRCh38
rs750938350	Chr.4: 41748485-41748485 on Build GRCh38
rs762144117	Chr.4: 41748446-41748446 on Build GRCh38
rs532711949	Chr.4: 41748384-41748384 on Build GRCh38
rs559227588	Chr.4: 41748465-41748465 on Build GRCh38
rs781024969	Chr.4: 41748398-41748399 on Build GRCh38
rs878854616	Chr.4: 41748476-41748476 on Build GRCh38
rs1012348354	Chr.4: 41748458-41748458 on Build GRCh38
rs774739194	Chr.4: 41748439-41748439 on Build GRCh38

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