Product Details

Primer Sequences

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Primer Chromosome Location

Chr.1: 216564160-216564389 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

ESRRG

Entrez Gene ID

2104

Gene Name

estrogen related receptor gamma

Gene Aliases

ERR3, ERRgamma, NR3B3

UniGene

Hs.444225

Gene Chromosome Location

Chr.1: 216503246-217137757 on Build GRCh38

Transcripts

NM_001134285.2 NM_001243505.1 NM_001243506.1 NM_001243507.1 NM_001243509.1 NM_001243510.2 NM_001243511.2 NM_001243512.1 NM_001243513.1 NM_001243514.1 NM_001243515.1 NM_001243518.1 NM_001243519.1 NM_001438.3 NM_206594.2 NM_206595.2 XM_011509265.2 XM_011509266.2 XM_011509267.1 XM_011509268.2 XM_011509269.2 XM_011509270.1 XM_011509271.2 XM_011509274.1 XM_011509275.1 XM_011509276.1 XM_011509277.1 XM_011509278.1 XM_011509279.1 XM_011509280.2 XM_017000621.1 XM_017000622.1 XM_017000623.1 XM_017000624.1 XM_017000625.1 XM_017000626.1 XM_017000627.1 XM_017000628.1 XM_017000629.1 XM_017000630.1 XM_017000631.1 XM_017000632.1 XM_017000633.1 XM_017000634.1 XM_017000635.1 XM_017000636.1 XM_017000637.1 XM_017000638.1 XM_017000639.1 XM_017000640.1 XM_017000641.1 XM_017000642.1 XM_017000643.1 XM_017000644.1 XM_017000645.1 XM_017000646.1 XM_017000647.1 XM_017000648.1 XM_017000649.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
146771	c.790G>T	p.A264S	Chr.1: 216564291-216564291 on Build GRCh38
5460759	c.773C>T	p.P258L	Chr.1: 216564308-216564308 on Build GRCh38
7234194	c.653A>G	p.D218G	Chr.1: 216564380-216564380 on Build GRCh38
4511018	c.819C>T	p.D273D	Chr.1: 216564262-216564262 on Build GRCh38
376529	c.756G>T	p.M252I	Chr.1: 216564325-216564325 on Build GRCh38
6061093	c.853C>A	p.H285N	Chr.1: 216564228-216564228 on Build GRCh38
6477580	c.742G>A	p.A248T	Chr.1: 216564291-216564291 on Build GRCh38
4811524	c.712G>A	p.D238N	Chr.1: 216564321-216564321 on Build GRCh38
6061091	c.801A>T	p.T267T	Chr.1: 216564280-216564280 on Build GRCh38
7234193	c.701A>G	p.Y234C	Chr.1: 216564380-216564380 on Build GRCh38
1338890	c.849G>A	p.A283A	Chr.1: 216564232-216564232 on Build GRCh38
4797976	c.799G>A	p.A267T	Chr.1: 216564234-216564234 on Build GRCh38
280872	c.721T>A	p.L241M	Chr.1: 216564360-216564360 on Build GRCh38
4231948	c.690G>A	p.P230P	Chr.1: 216564343-216564343 on Build GRCh38
4231945	c.704C>T	p.A235V	Chr.1: 216564329-216564329 on Build GRCh38
532581	c.738G>A	p.P246P	Chr.1: 216564343-216564343 on Build GRCh38
1295873	c.760G>A	p.D254N	Chr.1: 216564321-216564321 on Build GRCh38
4028263	c.805T>A	p.C269S	Chr.1: 216564276-216564276 on Build GRCh38
4783612	c.801G>A	p.A267A	Chr.1: 216564232-216564232 on Build GRCh38
2156182	c.701-1G>C	p.?	Chr.1: 216564381-216564381 on Build GRCh38
6061094	c.805C>A	p.H269N	Chr.1: 216564228-216564228 on Build GRCh38
678527	c.835A>G	p.I279V	Chr.1: 216564246-216564246 on Build GRCh38
4782281	c.742G>T	p.A248S	Chr.1: 216564291-216564291 on Build GRCh38
6061092	c.753A>T	p.T251T	Chr.1: 216564280-216564280 on Build GRCh38
4780198	c.811C>T	p.P271S	Chr.1: 216564222-216564222 on Build GRCh38
678526	c.815C>T	p.A272V	Chr.1: 216564266-216564266 on Build GRCh38
4028264	c.757T>A	p.C253S	Chr.1: 216564276-216564276 on Build GRCh38
678525	c.785T>C	p.I262T	Chr.1: 216564296-216564296 on Build GRCh38
5460760	c.725C>T	p.P242L	Chr.1: 216564308-216564308 on Build GRCh38
678524	c.730G>C	p.A244P	Chr.1: 216564351-216564351 on Build GRCh38
4797975	c.847G>A	p.A283T	Chr.1: 216564234-216564234 on Build GRCh38
6477579	c.790G>A	p.A264T	Chr.1: 216564291-216564291 on Build GRCh38
4681779	c.718A>T	p.T240S	Chr.1: 216564315-216564315 on Build GRCh38
3400331	c.652G>C	p.D218H	Chr.1: 216564381-216564381 on Build GRCh38
3376973	c.689C>T	p.P230L	Chr.1: 216564344-216564344 on Build GRCh38
1958530	c.752C>T	p.A251V	Chr.1: 216564329-216564329 on Build GRCh38
4862437	c.767C>T	p.A256V	Chr.1: 216564266-216564266 on Build GRCh38
3864513	c.846G>A	p.W282*	Chr.1: 216564235-216564235 on Build GRCh38
4861540	c.737T>C	p.I246T	Chr.1: 216564296-216564296 on Build GRCh38
4681778	c.766A>T	p.T256S	Chr.1: 216564315-216564315 on Build GRCh38
3376972	c.737C>T	p.P246L	Chr.1: 216564344-216564344 on Build GRCh38
4860078	c.682G>C	p.A228P	Chr.1: 216564351-216564351 on Build GRCh38
1626819	c.859C>T	p.P287S	Chr.1: 216564222-216564222 on Build GRCh38
4511019	c.771C>T	p.D257D	Chr.1: 216564262-216564262 on Build GRCh38
3864514	c.798G>A	p.W266*	Chr.1: 216564235-216564235 on Build GRCh38
4858853	c.787A>G	p.I263V	Chr.1: 216564246-216564246 on Build GRCh38
332807	c.853C>T	p.H285Y	Chr.1: 216564228-216564228 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs770733689	Chr.1: 216564300-216564300 on Build GRCh38
rs763892661	Chr.1: 216564189-216564189 on Build GRCh38
rs779064396	Chr.1: 216564256-216564256 on Build GRCh38
rs754403371	Chr.1: 216564242-216564242 on Build GRCh38
rs763664788	Chr.1: 216564344-216564344 on Build GRCh38
rs748236147	Chr.1: 216564258-216564258 on Build GRCh38
rs755377749	Chr.1: 216564244-216564244 on Build GRCh38
rs201736793	Chr.1: 216564265-216564265 on Build GRCh38
rs762615151	Chr.1: 216564343-216564343 on Build GRCh38
rs201435029	Chr.1: 216564332-216564332 on Build GRCh38
rs966328648	Chr.1: 216564310-216564310 on Build GRCh38
rs762859693	Chr.1: 216564252-216564252 on Build GRCh38
rs751248484	Chr.1: 216564211-216564211 on Build GRCh38
rs139709396	Chr.1: 216564259-216564259 on Build GRCh38
rs979981316	Chr.1: 216564313-216564313 on Build GRCh38
rs747209048	Chr.1: 216564285-216564285 on Build GRCh38
rs200261491	Chr.1: 216564306-216564306 on Build GRCh38
rs764293924	Chr.1: 216564192-216564192 on Build GRCh38
rs150595557	Chr.1: 216564307-216564307 on Build GRCh38
rs780520471	Chr.1: 216564232-216564232 on Build GRCh38
rs1036013279	Chr.1: 216564326-216564326 on Build GRCh38
rs756583718	Chr.1: 216564221-216564221 on Build GRCh38
rs970280342	Chr.1: 216564264-216564264 on Build GRCh38
rs149670038	Chr.1: 216564357-216564357 on Build GRCh38

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