Product Details

Primer Sequences

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Primer Chromosome Location

Chr.1: 159066001-159066270 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

AIM2

Entrez Gene ID

9447

Gene Name

absent in melanoma 2

Gene Aliases

PYHIN4

UniGene

Hs.733411

Gene Chromosome Location

Chr.1: 159059226-159132351 on Build GRCh38

Transcripts

NM_004833.1 XM_005245616.4 XM_017002848.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
676000	c.564C>T	p.F188F	Chr.1: 159066162-159066162 on Build GRCh38
318612	c.548C>A	p.T183K	Chr.1: 159066178-159066178 on Build GRCh38
4170561	c.521A>C	p.Q174P	Chr.1: 159066205-159066205 on Build GRCh38
278726	c.550G>T	p.E184*	Chr.1: 159066176-159066176 on Build GRCh38
5987770	c.700C>T	p.Q234*	Chr.1: 159066026-159066026 on Build GRCh38
6991966	c.506C>G	p.T169S	Chr.1: 159066220-159066220 on Build GRCh38
5378091	c.669C>G	p.S223R	Chr.1: 159066057-159066057 on Build GRCh38
3802417	c.545C>A	p.A182D	Chr.1: 159066181-159066181 on Build GRCh38
1666164	c.491C>G	p.P164R	Chr.1: 159066235-159066235 on Build GRCh38
897962	c.525G>T	p.E175D	Chr.1: 159066201-159066201 on Build GRCh38
1688881	c.556G>A	p.E186K	Chr.1: 159066170-159066170 on Build GRCh38
6507995	c.703A>T	p.K235*	Chr.1: 159066023-159066023 on Build GRCh38
897963	c.477G>A	p.L159L	Chr.1: 159066249-159066249 on Build GRCh38
1688880	c.575T>G	p.V192G	Chr.1: 159066151-159066151 on Build GRCh38
6597247	c.565T>G	p.F189V	Chr.1: 159066161-159066161 on Build GRCh38
1987301	c.677G>A	p.R226H	Chr.1: 159066049-159066049 on Build GRCh38
3863198	c.555G>A	p.K185K	Chr.1: 159066171-159066171 on Build GRCh38
6597248	c.486G>T	p.K162N	Chr.1: 159066240-159066240 on Build GRCh38
5479416	c.717G>A	p.P239P	Chr.1: 159066009-159066009 on Build GRCh38
3965934	c.669C>T	p.S223S	Chr.1: 159066057-159066057 on Build GRCh38
4951635	c.497C>G	p.T166R	Chr.1: 159066229-159066229 on Build GRCh38
4945741	c.578T>A	p.F193Y	Chr.1: 159066148-159066148 on Build GRCh38
1335316	c.593A>G	p.K198R	Chr.1: 159066133-159066133 on Build GRCh38
1335315	c.641G>A	p.R214Q	Chr.1: 159066085-159066085 on Build GRCh38
5007097	c.541G>C	p.V181L	Chr.1: 159066185-159066185 on Build GRCh38
897960	c.666T>C	p.N222N	Chr.1: 159066060-159066060 on Build GRCh38
372100	c.475C>A	p.L159M	Chr.1: 159066251-159066251 on Build GRCh38
897961	c.599A>C	p.K200T	Chr.1: 159066127-159066127 on Build GRCh38
3788902	c.612G>C	p.K204N	Chr.1: 159066114-159066114 on Build GRCh38
5341618	c.487A>C	p.K163Q	Chr.1: 159066239-159066239 on Build GRCh38
6459477	c.488A>G	p.K163R	Chr.1: 159066238-159066238 on Build GRCh38
3729153	c.603C>A	p.F201L	Chr.1: 159066123-159066123 on Build GRCh38
344861	c.689C>A	p.A230D	Chr.1: 159066037-159066037 on Build GRCh38
6058784	c.607C>A	p.P203T	Chr.1: 159066119-159066119 on Build GRCh38
1165683	c.670G>A	p.A224T	Chr.1: 159066056-159066056 on Build GRCh38
6058785	c.717G>T	p.P239P	Chr.1: 159066009-159066009 on Build GRCh38
7354969	c.658G>T	p.E220*	Chr.1: 159066068-159066068 on Build GRCh38
6121931	c.640C>G	p.R214G	Chr.1: 159066086-159066086 on Build GRCh38
4660664	c.590T>C	p.L197P	Chr.1: 159066136-159066136 on Build GRCh38
3476411	c.612G>A	p.K204K	Chr.1: 159066114-159066114 on Build GRCh38
6121930	c.492C>A	p.P164P	Chr.1: 159066234-159066234 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs761571921	Chr.1: 159066164-159066164 on Build GRCh38
rs760089097	Chr.1: 159066145-159066145 on Build GRCh38
rs770609652	Chr.1: 159066103-159066103 on Build GRCh38
rs373555103	Chr.1: 159066243-159066243 on Build GRCh38
rs756118457	Chr.1: 159066193-159066193 on Build GRCh38
rs376898750	Chr.1: 159066035-159066035 on Build GRCh38
rs35130877	Chr.1: 159066168-159066168 on Build GRCh38
rs756277653	Chr.1: 159066054-159066054 on Build GRCh38
rs772001101	Chr.1: 159066141-159066141 on Build GRCh38
rs572476207	Chr.1: 159066207-159066207 on Build GRCh38
rs148686373	Chr.1: 159066057-159066057 on Build GRCh38
rs969176404	Chr.1: 159066182-159066182 on Build GRCh38
rs368263314	Chr.1: 159066175-159066175 on Build GRCh38
rs775282472	Chr.1: 159066239-159066239 on Build GRCh38
rs866050462	Chr.1: 159066220-159066220 on Build GRCh38
rs375624593	Chr.1: 159066048-159066048 on Build GRCh38
rs774155198	Chr.1: 159066112-159066112 on Build GRCh38
rs375608638	Chr.1: 159066181-159066181 on Build GRCh38
rs763723491	Chr.1: 159066146-159066146 on Build GRCh38
rs745765084	Chr.1: 159066138-159066138 on Build GRCh38
rs774921419	Chr.1: 159066143-159066143 on Build GRCh38
rs545837561	Chr.1: 159066228-159066228 on Build GRCh38
rs539742230	Chr.1: 159066069-159066069 on Build GRCh38
rs771911036	Chr.1: 159066230-159066230 on Build GRCh38
rs369765206	Chr.1: 159066049-159066049 on Build GRCh38
rs944682755	Chr.1: 159066064-159066064 on Build GRCh38
rs745673444	Chr.1: 159066229-159066229 on Build GRCh38
rs200913901	Chr.1: 159066171-159066171 on Build GRCh38
rs765563535	Chr.1: 159066089-159066090 on Build GRCh38
rs749567312	Chr.1: 159066085-159066085 on Build GRCh38
rs1013616810	Chr.1: 159066159-159066159 on Build GRCh38
rs757503647	Chr.1: 159066216-159066216 on Build GRCh38
rs1052245685	Chr.1: 159066245-159066245 on Build GRCh38
rs768127211	Chr.1: 159066178-159066178 on Build GRCh38
rs373307771	Chr.1: 159066047-159066047 on Build GRCh38
rs748193319	Chr.1: 159066050-159066050 on Build GRCh38
rs776114459	Chr.1: 159066156-159066156 on Build GRCh38

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