Product Details

Primer Sequences

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Primer Chromosome Location

Chr.7: 69599675-69599924 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

AUTS2

Entrez Gene ID

26053

Gene Name

autism susceptibility candidate 2

Gene Aliases

FBRSL2, MRD26

UniGene

Hs.21631

Gene Chromosome Location

Chr.7: 69598475-70793068 on Build GRCh38

Transcripts

NM_001127231.2 NM_001127232.2 NM_015570.3 XM_011516010.2 XM_011516011.2 XM_011516012.2 XM_011516013.2 XM_011516014.2 XM_017011951.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
4646292	c.113G>A	p.G38D	Chr.7: 69599766-69599766 on Build GRCh38
6608927	c.166A>G	p.K56E	Chr.7: 69599819-69599819 on Build GRCh38
3086272	c.245C>A	p.S82*	Chr.7: 69599898-69599898 on Build GRCh38
3086271	c.245C>A	p.S82*	Chr.7: 69599898-69599898 on Build GRCh38
7284193	c.49C>T	p.R17W	Chr.7: 69599702-69599702 on Build GRCh38
3086264	c.212G>C	p.R71T	Chr.7: 69599865-69599865 on Build GRCh38
3086263	c.212G>C	p.R71T	Chr.7: 69599865-69599865 on Build GRCh38
6039522	c.231_232delGA	p.E79fs*10	Chr.7: 69599884-69599885 on Build GRCh38
5744933	c.217C>A	p.P73T	Chr.7: 69599870-69599870 on Build GRCh38
5662929	c.221G>T	p.R74L	Chr.7: 69599874-69599874 on Build GRCh38
5648368	c.100G>A	p.A34T	Chr.7: 69599753-69599753 on Build GRCh38
5648369	c.269G>A	p.G90E	Chr.7: 69599922-69599922 on Build GRCh38
7284194	c.49C>T	p.R17W	Chr.7: 69599702-69599702 on Build GRCh38
5076647	c.220C>T	p.R74W	Chr.7: 69599873-69599873 on Build GRCh38
6608908	c.205C>A	p.R69R	Chr.7: 69599858-69599858 on Build GRCh38
3882125	c.190T>C	p.S64P	Chr.7: 69599843-69599843 on Build GRCh38
3882124	c.190T>C	p.S64P	Chr.7: 69599843-69599843 on Build GRCh38
6608909	c.205C>A	p.R69R	Chr.7: 69599858-69599858 on Build GRCh38
4664766	c.221G>A	p.R74Q	Chr.7: 69599874-69599874 on Build GRCh38
3640165	c.199C>T	p.P67S	Chr.7: 69599852-69599852 on Build GRCh38
4664765	c.134C>T	p.A45V	Chr.7: 69599787-69599787 on Build GRCh38
4646291	c.113G>A	p.G38D	Chr.7: 69599766-69599766 on Build GRCh38
3086274	c.246G>A	p.S82S	Chr.7: 69599899-69599899 on Build GRCh38
3086273	c.246G>A	p.S82S	Chr.7: 69599899-69599899 on Build GRCh38
3640164	c.199C>T	p.P67S	Chr.7: 69599852-69599852 on Build GRCh38
3086268	c.219G>A	p.P73P	Chr.7: 69599872-69599872 on Build GRCh38
3086267	c.219G>A	p.P73P	Chr.7: 69599872-69599872 on Build GRCh38
3086261	c.205C>T	p.R69W	Chr.7: 69599858-69599858 on Build GRCh38
3086262	c.205C>T	p.R69W	Chr.7: 69599858-69599858 on Build GRCh38
5744934	c.217C>A	p.P73T	Chr.7: 69599870-69599870 on Build GRCh38
4434700	c.40C>T	p.R14W	Chr.7: 69599693-69599693 on Build GRCh38
4407905	c.206G>A	p.R69Q	Chr.7: 69599859-69599859 on Build GRCh38
5648370	c.269G>A	p.G90E	Chr.7: 69599922-69599922 on Build GRCh38
7205356	c.210C>T	p.P70P	Chr.7: 69599863-69599863 on Build GRCh38
5662928	c.221G>T	p.R74L	Chr.7: 69599874-69599874 on Build GRCh38
5648367	c.100G>A	p.A34T	Chr.7: 69599753-69599753 on Build GRCh38
7205357	c.210C>T	p.P70P	Chr.7: 69599863-69599863 on Build GRCh38
6039521	c.231_232delGA	p.E79fs*10	Chr.7: 69599884-69599885 on Build GRCh38
194768	c.206G>A	p.R69Q	Chr.7: 69599859-69599859 on Build GRCh38
3882127	c.255G>C	p.E85D	Chr.7: 69599908-69599908 on Build GRCh38
3882123	c.112G>A	p.G38S	Chr.7: 69599765-69599765 on Build GRCh38
6608928	c.166A>G	p.K56E	Chr.7: 69599819-69599819 on Build GRCh38
3882126	c.255G>C	p.E85D	Chr.7: 69599908-69599908 on Build GRCh38
3882122	c.112G>A	p.G38S	Chr.7: 69599765-69599765 on Build GRCh38
6548338	c.135G>T	p.A45A	Chr.7: 69599788-69599788 on Build GRCh38
4664764	c.134C>T	p.A45V	Chr.7: 69599787-69599787 on Build GRCh38
4434699	c.40C>T	p.R14W	Chr.7: 69599693-69599693 on Build GRCh38
6548337	c.135G>T	p.A45A	Chr.7: 69599788-69599788 on Build GRCh38
4664767	c.221G>A	p.R74Q	Chr.7: 69599874-69599874 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs762676699	Chr.7: 69599755-69599778 on Build GRCh38
rs945733678	Chr.7: 69599781-69599781 on Build GRCh38
rs911513762	Chr.7: 69599771-69599771 on Build GRCh38
rs753526278	Chr.7: 69599863-69599863 on Build GRCh38
rs777541048	Chr.7: 69599782-69599782 on Build GRCh38
rs1041469078	Chr.7: 69599787-69599787 on Build GRCh38
rs752490672	Chr.7: 69599750-69599773 on Build GRCh38
rs756779190	Chr.7: 69599784-69599784 on Build GRCh38
rs746774405	Chr.7: 69599806-69599806 on Build GRCh38
rs1001747687	Chr.7: 69599854-69599854 on Build GRCh38
rs750105505	Chr.7: 69599838-69599838 on Build GRCh38
rs1024257295	Chr.7: 69599858-69599858 on Build GRCh38
rs1004195592	Chr.7: 69599894-69599894 on Build GRCh38
rs756725295	Chr.7: 69599881-69599881 on Build GRCh38
rs780512031	Chr.7: 69599755-69599755 on Build GRCh38
rs775225727	Chr.7: 69599802-69599802 on Build GRCh38
rs761862785	Chr.7: 69599833-69599833 on Build GRCh38
rs755373797	Chr.7: 69599845-69599845 on Build GRCh38
rs776816196	Chr.7: 69599820-69599820 on Build GRCh38
rs910011165	Chr.7: 69599731-69599731 on Build GRCh38
rs771784577	Chr.7: 69599801-69599801 on Build GRCh38
rs763898324	Chr.7: 69599853-69599853 on Build GRCh38
rs552587555	Chr.7: 69599836-69599836 on Build GRCh38
rs1051354561	Chr.7: 69599761-69599761 on Build GRCh38
rs976017092	Chr.7: 69599743-69599743 on Build GRCh38
rs745753819	Chr.7: 69599798-69599798 on Build GRCh38
rs752423410	Chr.7: 69599765-69599765 on Build GRCh38
rs755792920	Chr.7: 69599780-69599780 on Build GRCh38
rs913230763	Chr.7: 69599727-69599727 on Build GRCh38
rs934214411	Chr.7: 69599759-69599759 on Build GRCh38
rs530867061	Chr.7: 69599740-69599740 on Build GRCh38
rs748798665	Chr.7: 69599783-69599783 on Build GRCh38
rs946041123	Chr.7: 69599815-69599815 on Build GRCh38
rs962834047	Chr.7: 69599733-69599733 on Build GRCh38
rs768911898	Chr.7: 69599810-69599810 on Build GRCh38
rs199945820	Chr.7: 69599841-69599841 on Build GRCh38
rs904301389	Chr.7: 69599794-69599794 on Build GRCh38
rs778785768	Chr.7: 69599797-69599797 on Build GRCh38

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