Product Details

Primer Sequences

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Primer Chromosome Location

Chr.2: 170996586-170996847 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

TLK1

Entrez Gene ID

9874

Gene Name

tousled like kinase 1

Gene Aliases

PKU-beta

UniGene

Hs.744917

Gene Chromosome Location

Chr.2: 170990823-171231314 on Build GRCh38

Transcripts

NM_001136554.1 NM_001136555.1 NM_012290.4 XM_011512238.2 XM_017005421.1 XM_017005422.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
7447361	c.2084T>C	p.V695A	Chr.2: 170996693-170996693 on Build GRCh38
6292933	c.2069T>A	p.L690*	Chr.2: 170996708-170996708 on Build GRCh38
7447362	c.1940T>C	p.V647A	Chr.2: 170996693-170996693 on Build GRCh38
6292934	c.1925T>A	p.L642*	Chr.2: 170996708-170996708 on Build GRCh38
1178626	c.1939G>C	p.V647L	Chr.2: 170996694-170996694 on Build GRCh38
7119600	c.2056G>C	p.E686Q	Chr.2: 170996721-170996721 on Build GRCh38
7119601	c.1912G>C	p.E638Q	Chr.2: 170996721-170996721 on Build GRCh38
1009481	c.2050C>A	p.L684I	Chr.2: 170996727-170996727 on Build GRCh38
6991879	c.2030A>G	p.N677S	Chr.2: 170996747-170996747 on Build GRCh38
1009482	c.1906C>A	p.L636I	Chr.2: 170996727-170996727 on Build GRCh38
164934	c.1977C>G	p.A659A	Chr.2: 170996656-170996656 on Build GRCh38
1178625	c.2083G>C	p.V695L	Chr.2: 170996694-170996694 on Build GRCh38
6991880	c.1886A>G	p.N629S	Chr.2: 170996747-170996747 on Build GRCh38
6456105	c.2107G>A	p.V703I	Chr.2: 170996670-170996670 on Build GRCh38
6456106	c.1963G>A	p.V655I	Chr.2: 170996670-170996670 on Build GRCh38
6434246	c.2054A>G	p.Q685R	Chr.2: 170996723-170996723 on Build GRCh38
4918160	c.1920A>G	p.T640T	Chr.2: 170996713-170996713 on Build GRCh38
6859866	c.2017-4_2017-3insT	p.?	Chr.2: 170996763-170996764 on Build GRCh38
6434247	c.1910A>G	p.Q637R	Chr.2: 170996723-170996723 on Build GRCh38
6859867	c.1873-4_1873-3insT	p.?	Chr.2: 170996763-170996764 on Build GRCh38
4086731	c.1936G>T	p.E646*	Chr.2: 170996697-170996697 on Build GRCh38
6423705	c.2102C>A	p.P701Q	Chr.2: 170996675-170996675 on Build GRCh38
6423706	c.1958C>A	p.P653Q	Chr.2: 170996675-170996675 on Build GRCh38
5991733	c.2017-4delT	p.?	Chr.2: 170996764-170996764 on Build GRCh38
5991734	c.1873-4delT	p.?	Chr.2: 170996764-170996764 on Build GRCh38
4918159	c.2064A>G	p.T688T	Chr.2: 170996713-170996713 on Build GRCh38
3723875	c.2051T>C	p.L684P	Chr.2: 170996726-170996726 on Build GRCh38
4809853	c.2121C>G	p.A707A	Chr.2: 170996656-170996656 on Build GRCh38
4086730	c.2080G>T	p.E694*	Chr.2: 170996697-170996697 on Build GRCh38
3723876	c.1907T>C	p.L636P	Chr.2: 170996726-170996726 on Build GRCh38
13369	c.1906C>T	p.L636F	Chr.2: 170996727-170996727 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs755326125	Chr.2: 170996771-170996775 on Build GRCh38
rs775832565	Chr.2: 170996634-170996634 on Build GRCh38
rs1045314	Chr.2: 170996719-170996719 on Build GRCh38
rs200299178	Chr.2: 170996635-170996635 on Build GRCh38
rs781461483	Chr.2: 170996778-170996782 on Build GRCh38
rs372222009	Chr.2: 170996609-170996609 on Build GRCh38
rs764357460	Chr.2: 170996637-170996637 on Build GRCh38
rs1042841965	Chr.2: 170996640-170996640 on Build GRCh38
rs747391375	Chr.2: 170996763-170996764 on Build GRCh38
rs374595379	Chr.2: 170996631-170996631 on Build GRCh38
rs774588067	Chr.2: 170996624-170996624 on Build GRCh38
rs564340817	Chr.2: 170996816-170996816 on Build GRCh38
rs558479097	Chr.2: 170996628-170996628 on Build GRCh38
rs751437890	Chr.2: 170996792-170996792 on Build GRCh38
rs748338332	Chr.2: 170996789-170996790 on Build GRCh38
rs1053319088	Chr.2: 170996814-170996815 on Build GRCh38
rs765979797	Chr.2: 170996787-170996787 on Build GRCh38
rs750147824	Chr.2: 170996764-170996764 on Build GRCh38
rs757727208	Chr.2: 170996686-170996686 on Build GRCh38
rs777065076	Chr.2: 170996647-170996647 on Build GRCh38
rs780545999	Chr.2: 170996764-170996764 on Build GRCh38
rs764930912	Chr.2: 170996749-170996749 on Build GRCh38
rs762296537	Chr.2: 170996683-170996683 on Build GRCh38

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