Product Details

Primer Sequences

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Primer Chromosome Location

Chr.9: 132905924-132906083 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

TSC1

Entrez Gene ID

7248

Gene Name

tuberous sclerosis 1

Gene Aliases

LAM, TSC

UniGene

Hs.370854

Gene Chromosome Location

Chr.9: 132891348-132945269 on Build GRCh38

Transcripts

NM_000368.4 NM_001162426.1 NM_001162427.1 XM_005272211.1 XM_006717271.1 XM_011518979.2 XM_017015096.1 XM_017015097.1 XM_017015098.1 XM_017015099.1 XM_017015100.1 XM_017015101.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
7347902	c.1624A>G	p.K542E	Chr.9: 132905954-132905954 on Build GRCh38
7408651	c.1598C>A	p.P533H	Chr.9: 132905980-132905980 on Build GRCh38
7347903	c.1643C>T	p.P548L	Chr.9: 132905935-132905935 on Build GRCh38
7347900	c.1538C>T	p.P513L	Chr.9: 132906040-132906040 on Build GRCh38
7347901	c.1571C>T	p.S524F	Chr.9: 132906007-132906007 on Build GRCh38
6942687	c.1525C>T	p.R509*	Chr.9: 132906053-132906053 on Build GRCh38
5946010	c.1579C>G	p.Q527E	Chr.9: 132905999-132905999 on Build GRCh38
5540955	c.1614C>T	p.S538S	Chr.9: 132905964-132905964 on Build GRCh38
6916214	c.1579C>T	p.Q527*	Chr.9: 132905999-132905999 on Build GRCh38
7347904	c.1646A>G	p.K549R	Chr.9: 132905932-132905932 on Build GRCh38
3996408	c.1591G>A	p.V531M	Chr.9: 132905987-132905987 on Build GRCh38
6927943	c.1625A>C	p.K542T	Chr.9: 132905953-132905953 on Build GRCh38
6982030	c.1636_1637delGA	p.D546fs*17	Chr.9: 132905941-132905942 on Build GRCh38
4736807	c.1564G>A	p.A522T	Chr.9: 132906014-132906014 on Build GRCh38
5415283	c.1498C>T	p.R500*	Chr.9: 132906080-132906080 on Build GRCh38
1330669	c.1587C>T	p.A529A	Chr.9: 132905991-132905991 on Build GRCh38
6946254	c.1549C>T	p.R517W	Chr.9: 132906029-132906029 on Build GRCh38
6023863	c.1566_1566delA	p.A523fs*9	Chr.9: 132906012-132906012 on Build GRCh38
3655165	c.1521T>C	p.F507F	Chr.9: 132906057-132906057 on Build GRCh38
307636	c.1546C>T	p.Q516*	Chr.9: 132906032-132906032 on Build GRCh38
1106328	c.1586C>T	p.A529V	Chr.9: 132905992-132905992 on Build GRCh38
607860	c.1584_1585CG>TT	p.A529S	Chr.9: 132905993-132905994 on Build GRCh38
7082054	c.1560C>T	p.H520H	Chr.9: 132906018-132906018 on Build GRCh38
6922847	c.1505G>A	p.G502D	Chr.9: 132906073-132906073 on Build GRCh38
7082053	c.1583G>A	p.G528D	Chr.9: 132905995-132905995 on Build GRCh38
7347889	c.1499G>A	p.R500Q	Chr.9: 132906079-132906079 on Build GRCh38
7347894	c.1616C>T	p.S539F	Chr.9: 132905962-132905962 on Build GRCh38
122140	c.1518C>G	p.P506P	Chr.9: 132906060-132906060 on Build GRCh38
1644123	c.?	p.L536Xfs*11	Chr.9: 132905971-132905972 on Build GRCh38
7112437	c.1510G>A	p.D504N	Chr.9: 132906068-132906068 on Build GRCh38
7347893	c.1517C>T	p.P506L	Chr.9: 132906061-132906061 on Build GRCh38
6957158	c.1583delG	p.G528fs*4	Chr.9: 132905995-132905995 on Build GRCh38
7347896	c.1513T>C	p.S505P	Chr.9: 132906065-132906065 on Build GRCh38
7346334	c.1516C>A	p.P506T	Chr.9: 132906062-132906062 on Build GRCh38
7347897	c.1596C>T	p.N532N	Chr.9: 132905982-132905982 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs118203544	Chr.9: 132906048-132906049 on Build GRCh38
rs765149885	Chr.9: 132905984-132905984 on Build GRCh38
rs118203542	Chr.9: 132906053-132906053 on Build GRCh38
rs371908551	Chr.9: 132906028-132906028 on Build GRCh38
rs118203546	Chr.9: 132906035-132906036 on Build GRCh38
rs756935981	Chr.9: 132905952-132905952 on Build GRCh38
rs776633158	Chr.9: 132905971-132905971 on Build GRCh38
rs118203543	Chr.9: 132906052-132906052 on Build GRCh38
rs281875358	Chr.9: 132906061-132906062 on Build GRCh38
rs397514810	Chr.9: 132906006-132906006 on Build GRCh38
rs751125011	Chr.9: 132905993-132905993 on Build GRCh38
rs796053458	Chr.9: 132905978-132905978 on Build GRCh38
rs372284519	Chr.9: 132905943-132905943 on Build GRCh38
rs770570830	Chr.9: 132905947-132905947 on Build GRCh38
rs878853961	Chr.9: 132905964-132905964 on Build GRCh38
rs898271020	Chr.9: 132905967-132905967 on Build GRCh38
rs878853960	Chr.9: 132906047-132906048 on Build GRCh38
rs118203551	Chr.9: 132905963-132905963 on Build GRCh38
rs397514823	Chr.9: 132906042-132906043 on Build GRCh38
rs118203549	Chr.9: 132905999-132905999 on Build GRCh38
rs377279170	Chr.9: 132905987-132905987 on Build GRCh38
rs118203548	Chr.9: 132906011-132906011 on Build GRCh38
rs118203540	Chr.9: 132906062-132906063 on Build GRCh38
rs368481360	Chr.9: 132905989-132905989 on Build GRCh38
rs779206386	Chr.9: 132906050-132906050 on Build GRCh38
rs759461471	Chr.9: 132905982-132905982 on Build GRCh38
rs749410972	Chr.9: 132906034-132906034 on Build GRCh38
rs118203545	Chr.9: 132906045-132906045 on Build GRCh38
rs767708806	Chr.9: 132905998-132905998 on Build GRCh38
rs118203550	Chr.9: 132905997-132905998 on Build GRCh38
rs766376606	Chr.9: 132905976-132905996 on Build GRCh38
rs755055358	Chr.9: 132906039-132906039 on Build GRCh38
rs750784794	Chr.9: 132906004-132906004 on Build GRCh38
rs762424091	Chr.9: 132905988-132905988 on Build GRCh38
rs149439187	Chr.9: 132905994-132905994 on Build GRCh38
rs118203547	Chr.9: 132906019-132906019 on Build GRCh38
rs759379027	Chr.9: 132906016-132906016 on Build GRCh38

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