Product Details

Primer Sequences

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Primer Chromosome Location

Chr.2: 118096588-118096835 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

INSIG2

Entrez Gene ID

51141

Gene Name

insulin induced gene 2

Gene Aliases

INSIG-2

UniGene

Hs.7089

Gene Chromosome Location

Chr.2: 118088418-118110031 on Build GRCh38

Transcripts

NM_001321329.1 NM_001321330.1 NM_001321331.1 NM_001321332.1 NM_001321333.1 NM_016133.3

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
4084419	c.187A>T	p.I63F	Chr.2: 118096743-118096743 on Build GRCh38
3961039	c.127G>T	p.A43S	Chr.2: 118096683-118096683 on Build GRCh38
6482774	c.95G>T	p.G32V	Chr.2: 118096651-118096651 on Build GRCh38
3836674	c.177A>C	p.P59P	Chr.2: 118096733-118096733 on Build GRCh38
6542969	c.148C>T	p.Q50*	Chr.2: 118096704-118096704 on Build GRCh38
6298412	c.186G>T	p.V62V	Chr.2: 118096742-118096742 on Build GRCh38
6308094	c.85A>T	p.M29L	Chr.2: 118096641-118096641 on Build GRCh38
475841	c.168G>A	p.T56T	Chr.2: 118096724-118096724 on Build GRCh38
1005867	c.72G>T	p.Q24H	Chr.2: 118096628-118096628 on Build GRCh38
4692646	c.167C>T	p.T56M	Chr.2: 118096723-118096723 on Build GRCh38
3040975	c.56C>T	p.S19L	Chr.2: 118096612-118096612 on Build GRCh38
3040976	c.106delT	p.F37fs*8	Chr.2: 118096662-118096662 on Build GRCh38
1752007	c.84G>T	p.L28F	Chr.2: 118096640-118096640 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs922095354	Chr.2: 118096627-118096627 on Build GRCh38
rs756111660	Chr.2: 118096688-118096688 on Build GRCh38
rs781017559	Chr.2: 118096656-118096656 on Build GRCh38
rs940346154	Chr.2: 118096775-118096775 on Build GRCh38
rs773442222	Chr.2: 118096769-118096769 on Build GRCh38
rs764572574	Chr.2: 118096777-118096777 on Build GRCh38
rs376950162	Chr.2: 118096724-118096724 on Build GRCh38
rs765415653	Chr.2: 118096674-118096674 on Build GRCh38
rs568055123	Chr.2: 118096786-118096786 on Build GRCh38
rs138954785	Chr.2: 118096727-118096727 on Build GRCh38
rs762335199	Chr.2: 118096703-118096704 on Build GRCh38
rs375348923	Chr.2: 118096622-118096622 on Build GRCh38
rs751179994	Chr.2: 118096796-118096796 on Build GRCh38
rs765960423	Chr.2: 118096615-118096615 on Build GRCh38
rs76370593	Chr.2: 118096800-118096800 on Build GRCh38
rs745585272	Chr.2: 118096792-118096792 on Build GRCh38
rs746239528	Chr.2: 118096734-118096734 on Build GRCh38
rs375157361	Chr.2: 118096793-118096793 on Build GRCh38
rs748170040	Chr.2: 118096669-118096669 on Build GRCh38
rs150499979	Chr.2: 118096707-118096707 on Build GRCh38
rs754766313	Chr.2: 118096631-118096631 on Build GRCh38
rs776841805	Chr.2: 118096700-118096701 on Build GRCh38
rs761312280	Chr.2: 118096752-118096752 on Build GRCh38
rs749320625	Chr.2: 118096723-118096723 on Build GRCh38
rs539714248	Chr.2: 118096742-118096742 on Build GRCh38
rs772723612	Chr.2: 118096790-118096790 on Build GRCh38
rs770287324	Chr.2: 118096705-118096706 on Build GRCh38
rs932227381	Chr.2: 118096721-118096721 on Build GRCh38
rs890738296	Chr.2: 118096745-118096745 on Build GRCh38
rs775687117	Chr.2: 118096749-118096749 on Build GRCh38
rs978916683	Chr.2: 118096624-118096624 on Build GRCh38

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