Product Details

Primer Sequences

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Primer Chromosome Location

Chr.13: 37021451-37021676 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

SUPT20H

Entrez Gene ID

55578

Gene Name

SPT20 homolog, SAGA complex component

Gene Aliases

C13, C13orf19, FAM48A, FP757, P38IP, SPT20

UniGene

Hs.435815

Gene Chromosome Location

Chr.13: 37009312-37059714 on Build GRCh38

Transcripts

NM_001014286.2 NM_001278480.1 NM_001278481.1 NM_001278482.1 NM_017569.3 XM_005266447.2 XM_005266449.3 XM_005266451.3 XM_005266454.3 XM_005266455.2 XM_005266456.3 XM_005266457.3 XM_005266458.3 XM_005266460.2 XM_005266461.3 XM_005266462.4 XM_005266464.3 XM_005266465.2 XM_005266467.3 XM_017020653.1 XM_017020654.1 XM_017020655.1 XM_017020656.1 XM_017020657.1 XM_017020658.1 XM_017020659.1 XM_017020660.1 XM_017020661.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6483772	c.1665G>T	p.G555G	Chr.13: 37021599-37021599 on Build GRCh38
6580631	c.1801C>T	p.Q601*	Chr.13: 37021466-37021466 on Build GRCh38
696644	c.1664G>A	p.G555E	Chr.13: 37021600-37021600 on Build GRCh38
6139296	c.1753C>G	p.L585V	Chr.13: 37021511-37021511 on Build GRCh38
6521006	c.1664G>T	p.G555V	Chr.13: 37021600-37021600 on Build GRCh38
947167	c.1797G>A	p.M599I	Chr.13: 37021467-37021467 on Build GRCh38
6483774	c.1663G>T	p.G555W	Chr.13: 37021601-37021601 on Build GRCh38
4867800	c.1800G>A	p.M600I	Chr.13: 37021467-37021467 on Build GRCh38
6483773	c.1668G>T	p.G556G	Chr.13: 37021599-37021599 on Build GRCh38
6139297	c.1756C>G	p.L586V	Chr.13: 37021511-37021511 on Build GRCh38
6521007	c.1667G>T	p.G556V	Chr.13: 37021600-37021600 on Build GRCh38
6483775	c.1666G>T	p.G556W	Chr.13: 37021601-37021601 on Build GRCh38
4619695	c.1777A>G	p.N593D	Chr.13: 37021487-37021487 on Build GRCh38
6402169	c.1733G>T	p.G578V	Chr.13: 37021531-37021531 on Build GRCh38
1629087	c.1799A>G	p.Q600R	Chr.13: 37021465-37021465 on Build GRCh38
5017181	c.1763G>A	p.G588E	Chr.13: 37021501-37021501 on Build GRCh38
3711058	c.1766G>A	p.G589D	Chr.13: 37021498-37021498 on Build GRCh38
3718461	c.1769G>A	p.G590D	Chr.13: 37021498-37021498 on Build GRCh38
4863232	c.1667G>A	p.G556E	Chr.13: 37021600-37021600 on Build GRCh38
6580630	c.1798C>T	p.Q600*	Chr.13: 37021466-37021466 on Build GRCh38
6402170	c.1736G>T	p.G579V	Chr.13: 37021531-37021531 on Build GRCh38
5017182	c.1766G>A	p.G589E	Chr.13: 37021501-37021501 on Build GRCh38
4619696	c.1780A>G	p.N594D	Chr.13: 37021487-37021487 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs755314663	Chr.13: 37021503-37021503 on Build GRCh38
rs779204624	Chr.13: 37021504-37021504 on Build GRCh38
rs766121706	Chr.13: 37021505-37021505 on Build GRCh38
rs780738673	Chr.13: 37021557-37021557 on Build GRCh38
rs1046838310	Chr.13: 37021501-37021501 on Build GRCh38
rs199796421	Chr.13: 37021517-37021517 on Build GRCh38
rs952919870	Chr.13: 37021482-37021482 on Build GRCh38
rs762614387	Chr.13: 37021610-37021610 on Build GRCh38
rs768534321	Chr.13: 37021630-37021630 on Build GRCh38
rs758816969	Chr.13: 37021518-37021518 on Build GRCh38
rs760465730	Chr.13: 37021485-37021485 on Build GRCh38
rs775230282	Chr.13: 37021594-37021594 on Build GRCh38
rs778105167	Chr.13: 37021524-37021524 on Build GRCh38
rs554703387	Chr.13: 37021638-37021638 on Build GRCh38
rs144899348	Chr.13: 37021567-37021567 on Build GRCh38
rs777339871	Chr.13: 37021646-37021647 on Build GRCh38
rs770406704	Chr.13: 37021553-37021553 on Build GRCh38
rs929696737	Chr.13: 37021499-37021499 on Build GRCh38
rs760803976	Chr.13: 37021480-37021480 on Build GRCh38
rs142518257	Chr.13: 37021537-37021537 on Build GRCh38
rs111384116	Chr.13: 37021473-37021473 on Build GRCh38
rs188364760	Chr.13: 37021495-37021495 on Build GRCh38
rs965419464	Chr.13: 37021509-37021509 on Build GRCh38
rs769272648	Chr.13: 37021574-37021574 on Build GRCh38
rs9603129	Chr.13: 37021565-37021565 on Build GRCh38
rs1018361579	Chr.13: 37021506-37021506 on Build GRCh38
rs761896125	Chr.13: 37021650-37021650 on Build GRCh38

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