Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.11: 36490072-36490345 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: TRAF6
Entrez Gene ID: 7189
Gene Name: TNF receptor associated factor 6
Gene Aliases: MGC:3310, RNF85
UniGene: Hs.444172
Gene Chromosome Location: Chr.11: 36483767-36510313 on Build GRCh38
Transcripts: NM_004620.3 NM_145803.2

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
5014988	c.1204C>T	p.R402C	Chr.11: 36490203-36490203 on Build GRCh38
926723	c.1214A>G	p.N405S	Chr.11: 36490193-36490193 on Build GRCh38
926722	c.1303C>A	p.L435I	Chr.11: 36490104-36490104 on Build GRCh38
3447041	c.1126C>T	p.H376Y	Chr.11: 36490281-36490281 on Build GRCh38
3447040	c.1266C>T	p.L422L	Chr.11: 36490141-36490141 on Build GRCh38
370398	c.1193C>T	p.P398L	Chr.11: 36490214-36490214 on Build GRCh38
5372412	c.1233C>T	p.V411V	Chr.11: 36490174-36490174 on Build GRCh38
1353711	c.1194G>A	p.P398P	Chr.11: 36490213-36490213 on Build GRCh38
6132410	c.1324G>T	p.V442L	Chr.11: 36490083-36490083 on Build GRCh38
4574348	c.1321C>A	p.P441T	Chr.11: 36490086-36490086 on Build GRCh38
3447039	c.1268C>T	p.P423L	Chr.11: 36490139-36490139 on Build GRCh38
6328664	c.1201C>T	p.Q401*	Chr.11: 36490206-36490206 on Build GRCh38
328289	c.1313C>G	p.S438C	Chr.11: 36490094-36490094 on Build GRCh38
5946991	c.1064G>A	p.W355*	Chr.11: 36490343-36490343 on Build GRCh38
428952	c.1105G>A	p.E369K	Chr.11: 36490302-36490302 on Build GRCh38
4185604	c.1264C>A	p.L422I	Chr.11: 36490143-36490143 on Build GRCh38
687421	c.1242G>A	p.M414I	Chr.11: 36490165-36490165 on Build GRCh38
1978206	c.1174C>T	p.R392C	Chr.11: 36490233-36490233 on Build GRCh38
4462930	c.1267C>T	p.P423S	Chr.11: 36490140-36490140 on Build GRCh38
4394442	c.1225C>T	p.L409F	Chr.11: 36490182-36490182 on Build GRCh38
212503	c.1175G>A	p.R392H	Chr.11: 36490232-36490232 on Build GRCh38
5999709	c.1171A>G	p.M391V	Chr.11: 36490236-36490236 on Build GRCh38
5473124	c.1156G>A	p.G386R	Chr.11: 36490251-36490251 on Build GRCh38
1703817	c.1303C>T	p.L435F	Chr.11: 36490104-36490104 on Build GRCh38
6870771	c.1328G>A	p.R443K	Chr.11: 36490079-36490079 on Build GRCh38
5666999	c.1144A>T	p.T382S	Chr.11: 36490263-36490263 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs949300138	Chr.11: 36490156-36490156 on Build GRCh38
rs777821743	Chr.11: 36490252-36490252 on Build GRCh38
rs761368102	Chr.11: 36490149-36490149 on Build GRCh38
rs536779653	Chr.11: 36490294-36490294 on Build GRCh38
rs764878622	Chr.11: 36490150-36490150 on Build GRCh38
rs144270884	Chr.11: 36490261-36490261 on Build GRCh38
rs199830912	Chr.11: 36490202-36490202 on Build GRCh38
rs916447705	Chr.11: 36490148-36490148 on Build GRCh38
rs747509379	Chr.11: 36490321-36490321 on Build GRCh38
rs746111041	Chr.11: 36490302-36490302 on Build GRCh38
rs34165477	Chr.11: 36490221-36490222 on Build GRCh38
rs754966271	Chr.11: 36490231-36490231 on Build GRCh38
rs187625425	Chr.11: 36490258-36490258 on Build GRCh38
rs200661146	Chr.11: 36490107-36490107 on Build GRCh38
rs772536661	Chr.11: 36490303-36490303 on Build GRCh38
rs776263136	Chr.11: 36490119-36490119 on Build GRCh38
rs750059919	Chr.11: 36490183-36490183 on Build GRCh38
rs776049763	Chr.11: 36490316-36490316 on Build GRCh38
rs751475632	Chr.11: 36490213-36490213 on Build GRCh38
rs548543739	Chr.11: 36490203-36490203 on Build GRCh38

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