Product Details

Primer Sequences

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Primer Chromosome Location

Chr.17: 76904271-76904496 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

MGAT5B

Entrez Gene ID

146664

Gene Name

mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B

Gene Aliases

GnT-IX, GnT-VB

UniGene

Hs.144531

Gene Chromosome Location

Chr.17: 76868487-76950389 on Build GRCh38

Transcripts

NM_001199172.1 NM_144677.2 NM_198955.1 XM_006721707.3 XM_011524350.2 XM_011524352.2 XM_011524354.2 XM_017024200.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
5561915	c.673C>A	p.P225T	Chr.17: 76904405-76904405 on Build GRCh38
5565033	c.694A>G	p.R232G	Chr.17: 76904393-76904393 on Build GRCh38
6081964	c.589T>C	p.F197L	Chr.17: 76904321-76904321 on Build GRCh38
7377094	c.689C>G	p.A230G	Chr.17: 76904388-76904388 on Build GRCh38
6081963	c.622T>C	p.F208L	Chr.17: 76904321-76904321 on Build GRCh38
5561914	c.706C>A	p.P236T	Chr.17: 76904405-76904405 on Build GRCh38
5510940	c.630G>A	p.P210P	Chr.17: 76904362-76904362 on Build GRCh38
6712311	c.675G>C	p.R225S	Chr.17: 76904374-76904374 on Build GRCh38
1386266	c.641G>T	p.R214M	Chr.17: 76904373-76904373 on Build GRCh38
6368542	c.671G>A	p.W224*	Chr.17: 76904370-76904370 on Build GRCh38
3403246	c.643G>A	p.V215I	Chr.17: 76904342-76904342 on Build GRCh38
6712312	c.642G>C	p.R214S	Chr.17: 76904374-76904374 on Build GRCh38
5510939	c.663G>A	p.P221P	Chr.17: 76904362-76904362 on Build GRCh38
6368543	c.638G>A	p.W213*	Chr.17: 76904370-76904370 on Build GRCh38
1386265	c.623_624insC	p.L211fs*133	Chr.17: 76904355-76904356 on Build GRCh38
3820669	c.620C>G	p.S207C	Chr.17: 76904319-76904319 on Build GRCh38
5892333	c.688C>T	p.Q230*	Chr.17: 76904420-76904420 on Build GRCh38
3672585	c.574G>T	p.G192C	Chr.17: 76904306-76904306 on Build GRCh38
5892332	c.721C>T	p.Q241*	Chr.17: 76904420-76904420 on Build GRCh38
4503677	c.645C>T	p.V215V	Chr.17: 76904344-76904344 on Build GRCh38
6322211	c.618G>T	p.W206C	Chr.17: 76904350-76904350 on Build GRCh38
1303391	c.594C>T	p.L198L	Chr.17: 76904326-76904326 on Build GRCh38
6322210	c.651G>T	p.W217C	Chr.17: 76904350-76904350 on Build GRCh38
4502849	c.624C>T	p.F208F	Chr.17: 76904323-76904323 on Build GRCh38
1589209	c.594C>A	p.F198L	Chr.17: 76904293-76904293 on Build GRCh38
5028373	c.644A>G	p.N215S	Chr.17: 76904376-76904376 on Build GRCh38
3672584	c.607G>T	p.G203C	Chr.17: 76904306-76904306 on Build GRCh38
5111152	c.656_657insC	p.L222fs*133	Chr.17: 76904355-76904356 on Build GRCh38
5099281	c.674G>T	p.R225M	Chr.17: 76904373-76904373 on Build GRCh38
5661233	c.686T>A	p.V229D	Chr.17: 76904418-76904418 on Build GRCh38
984791	c.561C>A	p.F187L	Chr.17: 76904293-76904293 on Build GRCh38
6556691	c.690C>T	p.A230A	Chr.17: 76904389-76904389 on Build GRCh38
6556692	c.657C>T	p.A219A	Chr.17: 76904389-76904389 on Build GRCh38
7085027	c.627C>T	p.L209L	Chr.17: 76904326-76904326 on Build GRCh38
5661232	c.719T>A	p.V240D	Chr.17: 76904418-76904418 on Build GRCh38
342242	c.570G>T	p.V190V	Chr.17: 76904302-76904302 on Build GRCh38
5028372	c.677A>G	p.N226S	Chr.17: 76904376-76904376 on Build GRCh38
4503678	c.612C>T	p.V204V	Chr.17: 76904344-76904344 on Build GRCh38
3820670	c.587C>G	p.S196C	Chr.17: 76904319-76904319 on Build GRCh38
3403247	c.610G>A	p.V204I	Chr.17: 76904342-76904342 on Build GRCh38
5565034	c.661A>G	p.R221G	Chr.17: 76904393-76904393 on Build GRCh38
4502850	c.591C>T	p.F197F	Chr.17: 76904323-76904323 on Build GRCh38
7377095	c.656C>G	p.A219G	Chr.17: 76904388-76904388 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs146591034	Chr.17: 76904401-76904401 on Build GRCh38
rs190033210	Chr.17: 76904361-76904361 on Build GRCh38
rs201242038	Chr.17: 76904311-76904311 on Build GRCh38
rs1018418061	Chr.17: 76904440-76904440 on Build GRCh38
rs753041621	Chr.17: 76904356-76904356 on Build GRCh38
rs369169563	Chr.17: 76904312-76904312 on Build GRCh38
rs543125188	Chr.17: 76904426-76904426 on Build GRCh38
rs11650151	Chr.17: 76904301-76904301 on Build GRCh38
rs761836889	Chr.17: 76904447-76904447 on Build GRCh38
rs775603524	Chr.17: 76904410-76904410 on Build GRCh38
rs760389297	Chr.17: 76904290-76904290 on Build GRCh38
rs376928919	Chr.17: 76904397-76904397 on Build GRCh38
rs140471018	Chr.17: 76904329-76904329 on Build GRCh38
rs377122452	Chr.17: 76904349-76904349 on Build GRCh38
rs999682478	Chr.17: 76904368-76904368 on Build GRCh38
rs372736073	Chr.17: 76904344-76904344 on Build GRCh38
rs778961529	Chr.17: 76904388-76904388 on Build GRCh38
rs764051103	Chr.17: 76904305-76904305 on Build GRCh38
rs746765660	Chr.17: 76904436-76904436 on Build GRCh38
rs778294137	Chr.17: 76904378-76904378 on Build GRCh38
rs903325130	Chr.17: 76904345-76904345 on Build GRCh38
rs1013237874	Chr.17: 76904430-76904430 on Build GRCh38
rs772789731	Chr.17: 76904460-76904460 on Build GRCh38
rs200272265	Chr.17: 76904446-76904446 on Build GRCh38
rs61736672	Chr.17: 76904383-76904383 on Build GRCh38
rs369519601	Chr.17: 76904382-76904382 on Build GRCh38
rs1032088398	Chr.17: 76904387-76904387 on Build GRCh38
rs775345454	Chr.17: 76904288-76904288 on Build GRCh38
rs59862466	Chr.17: 76904465-76904465 on Build GRCh38
rs772211704	Chr.17: 76904407-76904407 on Build GRCh38
rs1046291792	Chr.17: 76904364-76904364 on Build GRCh38
rs553577630	Chr.17: 76904306-76904306 on Build GRCh38
rs768310072	Chr.17: 76904438-76904438 on Build GRCh38
rs750021114	Chr.17: 76904332-76904332 on Build GRCh38

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