Product Details

Primer Sequences

Log in to view

Primer Chromosome Location

Chr.7: 69599595-69599830 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

View Less

Cosmic ID	Mutation	AA	Transcript Location
4646292	c.113G>A	p.G38D	Chr.7: 69599766-69599766 on Build GRCh38
3750042	c.11C>T	p.P4L	Chr.7: 69599664-69599664 on Build GRCh38
6608927	c.166A>G	p.K56E	Chr.7: 69599819-69599819 on Build GRCh38
4635529	c.15G>A	p.T5T	Chr.7: 69599668-69599668 on Build GRCh38
4635528	c.15G>A	p.T5T	Chr.7: 69599668-69599668 on Build GRCh38
6608928	c.166A>G	p.K56E	Chr.7: 69599819-69599819 on Build GRCh38
3882123	c.112G>A	p.G38S	Chr.7: 69599765-69599765 on Build GRCh38
7284193	c.49C>T	p.R17W	Chr.7: 69599702-69599702 on Build GRCh38
3750043	c.11C>T	p.P4L	Chr.7: 69599664-69599664 on Build GRCh38
3882122	c.112G>A	p.G38S	Chr.7: 69599765-69599765 on Build GRCh38
4434700	c.40C>T	p.R14W	Chr.7: 69599693-69599693 on Build GRCh38
6548338	c.135G>T	p.A45A	Chr.7: 69599788-69599788 on Build GRCh38
6419453	c.14C>A	p.T5K	Chr.7: 69599667-69599667 on Build GRCh38
5648368	c.100G>A	p.A34T	Chr.7: 69599753-69599753 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
6419452	c.14C>A	p.T5K	Chr.7: 69599667-69599667 on Build GRCh38
6548337	c.135G>T	p.A45A	Chr.7: 69599788-69599788 on Build GRCh38
7284194	c.49C>T	p.R17W	Chr.7: 69599702-69599702 on Build GRCh38
5648367	c.100G>A	p.A34T	Chr.7: 69599753-69599753 on Build GRCh38
4646291	c.113G>A	p.G38D	Chr.7: 69599766-69599766 on Build GRCh38
4664765	c.134C>T	p.A45V	Chr.7: 69599787-69599787 on Build GRCh38

View More

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
rs777541048	Chr.7: 69599782-69599782 on Build GRCh38
rs752490672	Chr.7: 69599750-69599773 on Build GRCh38
rs1041469078	Chr.7: 69599787-69599787 on Build GRCh38
rs1041341061	Chr.7: 69599668-69599668 on Build GRCh38
rs891065709	Chr.7: 69599633-69599633 on Build GRCh38
rs756779190	Chr.7: 69599784-69599784 on Build GRCh38
rs746774405	Chr.7: 69599806-69599806 on Build GRCh38
rs780512031	Chr.7: 69599755-69599755 on Build GRCh38
rs775225727	Chr.7: 69599802-69599802 on Build GRCh38
rs200189077	Chr.7: 69599664-69599664 on Build GRCh38
rs910011165	Chr.7: 69599731-69599731 on Build GRCh38
rs3735260	Chr.7: 69599651-69599651 on Build GRCh38
rs771784577	Chr.7: 69599801-69599801 on Build GRCh38
rs1051354561	Chr.7: 69599761-69599761 on Build GRCh38
rs976017092	Chr.7: 69599743-69599743 on Build GRCh38
rs752423410	Chr.7: 69599765-69599765 on Build GRCh38
rs745753819	Chr.7: 69599798-69599798 on Build GRCh38
rs755792920	Chr.7: 69599780-69599780 on Build GRCh38
rs934214411	Chr.7: 69599759-69599759 on Build GRCh38
rs913230763	Chr.7: 69599727-69599727 on Build GRCh38
rs530867061	Chr.7: 69599740-69599740 on Build GRCh38
rs534062236	Chr.7: 69599612-69599612 on Build GRCh38
rs748798665	Chr.7: 69599783-69599783 on Build GRCh38
rs904301389	Chr.7: 69599794-69599794 on Build GRCh38
rs768911898	Chr.7: 69599810-69599810 on Build GRCh38
rs962834047	Chr.7: 69599733-69599733 on Build GRCh38
rs778785768	Chr.7: 69599797-69599797 on Build GRCh38

View Full Product Details