Product Details

Primer Sequences

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Primer Chromosome Location

Chr.17: 49618844-49619109 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

SPOP

Entrez Gene ID

8405

Gene Name

speckle type BTB/POZ protein

Gene Aliases

BTBD32, TEF2

UniGene

Hs.463382

Gene Chromosome Location

Chr.17: 49598884-49678163 on Build GRCh38

Transcripts

NM_001007226.1 NM_001007227.1 NM_001007228.1 NM_001007229.1 NM_001007230.1 NM_003563.3 XM_005257723.4 XM_005257724.4 XM_017025204.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
3728329	c.413G>C	p.R138P	Chr.17: 49619048-49619048 on Build GRCh38
4729697	c.412C>T	p.R138C	Chr.17: 49619049-49619049 on Build GRCh38
95272	c.399C>G	p.F133L	Chr.17: 49619062-49619062 on Build GRCh38
1290717	c.388G>A	p.D130N	Chr.17: 49619073-49619073 on Build GRCh38
5821809	c.457G>T	p.D153Y	Chr.17: 49619004-49619004 on Build GRCh38
6916242	c.374T>G	p.F125C	Chr.17: 49619087-49619087 on Build GRCh38
6935857	c.445C>T	p.L149F	Chr.17: 49619016-49619016 on Build GRCh38
242641	c.391T>G	p.W131G	Chr.17: 49619070-49619070 on Build GRCh38
980811	c.362G>A	p.R121Q	Chr.17: 49619099-49619099 on Build GRCh38
5013192	c.371G>C	p.R124T	Chr.17: 49619090-49619090 on Build GRCh38
6970595	c.467C>T	p.T156I	Chr.17: 49618994-49618994 on Build GRCh38
980809	c.418G>A	p.D140N	Chr.17: 49619043-49619043 on Build GRCh38
5964358	c.480+7C>T	p.?	Chr.17: 49618974-49618974 on Build GRCh38
3749406	c.424C>T	p.L142F	Chr.17: 49619037-49619037 on Build GRCh38
6929898	c.392G>T	p.W131L	Chr.17: 49619069-49619069 on Build GRCh38
247573	c.398T>C	p.F133S	Chr.17: 49619063-49619063 on Build GRCh38
5414952	c.395G>A	p.G132E	Chr.17: 49619066-49619066 on Build GRCh38
247571	c.399C>A	p.F133L	Chr.17: 49619062-49619062 on Build GRCh38
6938938	c.413G>A	p.R138H	Chr.17: 49619048-49619048 on Build GRCh38
242644	c.402G>C	p.K134N	Chr.17: 49619059-49619059 on Build GRCh38
5759035	c.419A>C	p.D140A	Chr.17: 49619042-49619042 on Build GRCh38
4420882	c.406T>C	p.F136L	Chr.17: 49619055-49619055 on Build GRCh38
6957596	c.402G>T	p.K134N	Chr.17: 49619059-49619059 on Build GRCh38
2698399	c.388G>C	p.D130H	Chr.17: 49619073-49619073 on Build GRCh38
6951977	c.375T>G	p.F125L	Chr.17: 49619086-49619086 on Build GRCh38
4392689	c.397T>C	p.F133L	Chr.17: 49619064-49619064 on Build GRCh38
6789220	c.423delT	p.L142fs*20	Chr.17: 49619038-49619038 on Build GRCh38
5909633	c.448C>T	p.L150F	Chr.17: 49619013-49619013 on Build GRCh38
3672490	c.392G>C	p.W131S	Chr.17: 49619069-49619069 on Build GRCh38
95273	c.373T>G	p.F125V	Chr.17: 49619088-49619088 on Build GRCh38
4729696	c.424C>A	p.L142I	Chr.17: 49619037-49619037 on Build GRCh38
5414797	c.457G>A	p.D153N	Chr.17: 49619004-49619004 on Build GRCh38
242642	c.385A>G	p.K129E	Chr.17: 49619076-49619076 on Build GRCh38
3819898	c.353-1G>A	p.?	Chr.17: 49619109-49619109 on Build GRCh38
980810	c.393G>T	p.W131C	Chr.17: 49619068-49619068 on Build GRCh38
241745	c.364_366delGCA	p.A122delA	Chr.17: 49619095-49619097 on Build GRCh38
980808	c.419A>G	p.D140G	Chr.17: 49619042-49619042 on Build GRCh38
219965	c.397T>G	p.F133V	Chr.17: 49619064-49619064 on Build GRCh38
6932260	c.382G>A	p.G128S	Chr.17: 49619079-49619079 on Build GRCh38
5414953	c.355A>G	p.S119G	Chr.17: 49619106-49619106 on Build GRCh38
247572	c.356G>A	p.S119N	Chr.17: 49619105-49619105 on Build GRCh38
6939088	c.436G>A	p.A146T	Chr.17: 49619025-49619025 on Build GRCh38
242645	c.398T>G	p.F133C	Chr.17: 49619063-49619063 on Build GRCh38
5414798	c.358C>T	p.Q120*	Chr.17: 49619103-49619103 on Build GRCh38
242643	c.375T>A	p.F125L	Chr.17: 49619086-49619086 on Build GRCh38
1130239	c.391T>C	p.W131R	Chr.17: 49619070-49619070 on Build GRCh38
6904352	c.361C>G	p.R121G	Chr.17: 49619100-49619100 on Build GRCh38
2698401	c.361C>T	p.R121W	Chr.17: 49619100-49619100 on Build GRCh38
4420161	c.397T>A	p.F133I	Chr.17: 49619064-49619064 on Build GRCh38
2698398	c.431A>G	p.D144G	Chr.17: 49619030-49619030 on Build GRCh38
6955236	c.404A>C	p.K135T	Chr.17: 49619057-49619057 on Build GRCh38
5415481	c.393G>C	p.W131C	Chr.17: 49619068-49619068 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs777389504	Chr.17: 49619083-49619083 on Build GRCh38
rs113265648	Chr.17: 49619027-49619027 on Build GRCh38
rs184050028	Chr.17: 49618918-49618918 on Build GRCh38
rs1006096444	Chr.17: 49619057-49619057 on Build GRCh38
rs375093038	Chr.17: 49618984-49618984 on Build GRCh38
rs968974699	Chr.17: 49619049-49619049 on Build GRCh38
rs764345128	Chr.17: 49618958-49618958 on Build GRCh38
rs1041177741	Chr.17: 49618920-49618920 on Build GRCh38
rs189515524	Chr.17: 49618945-49618945 on Build GRCh38
rs1036158089	Chr.17: 49618932-49618932 on Build GRCh38
rs762189786	Chr.17: 49618969-49618969 on Build GRCh38
rs755810590	Chr.17: 49619053-49619053 on Build GRCh38
rs754476215	Chr.17: 49618990-49618990 on Build GRCh38
rs193921065	Chr.17: 49619062-49619062 on Build GRCh38
rs760999631	Chr.17: 49618949-49618949 on Build GRCh38
rs914728063	Chr.17: 49619044-49619044 on Build GRCh38
rs767050824	Chr.17: 49619020-49619020 on Build GRCh38
rs752320964	Chr.17: 49619038-49619038 on Build GRCh38
rs930051780	Chr.17: 49618961-49618961 on Build GRCh38
rs775851222	Chr.17: 49618946-49618946 on Build GRCh38
rs762440331	Chr.17: 49618924-49618924 on Build GRCh38
rs745957392	Chr.17: 49618940-49618940 on Build GRCh38
rs981559838	Chr.17: 49618872-49618872 on Build GRCh38
rs777079703	Chr.17: 49618968-49618968 on Build GRCh38
rs368288966	Chr.17: 49618987-49618987 on Build GRCh38
rs888419251	Chr.17: 49619047-49619047 on Build GRCh38

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