Product Details

Primer Sequences

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Primer Chromosome Location

Chr.2: 15942201-15942468 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

MYCN

Entrez Gene ID

4613

Gene Name

v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog

Gene Aliases

MODED, N-myc, NMYC, ODED, bHLHe37

UniGene

Hs.25960

Gene Chromosome Location

Chr.2: 15940438-15947007 on Build GRCh38

Transcripts

NM_001293228.1 NM_001293231.1 NM_001293233.1 NM_005378.5 XM_017004168.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
717282	c.333C>T	p.I111I	Chr.2: 15942397-15942397 on Build GRCh38
717284	c.225G>T	p.P75P	Chr.2: 15942289-15942289 on Build GRCh38
6956858	c.175delC	p.P60fs*71	Chr.2: 15942239-15942239 on Build GRCh38
5899859	c.179C>T	p.P60L	Chr.2: 15942243-15942243 on Build GRCh38
1668725	c.170C>A	p.P57H	Chr.2: 15942234-15942234 on Build GRCh38
5911691	c.178C>T	p.P60S	Chr.2: 15942242-15942242 on Build GRCh38
4778545	c.205G>A	p.E69K	Chr.2: 15942269-15942269 on Build GRCh38
3798087	c.370G>A	p.E124K	Chr.2: 15942434-15942434 on Build GRCh38
5924942	c.176C>T	p.P59L	Chr.2: 15942240-15942240 on Build GRCh38
4883721	c.208C>A	p.H70N	Chr.2: 15942272-15942272 on Build GRCh38
7275711	c.312C>T	p.G104G	Chr.2: 15942376-15942376 on Build GRCh38
4582734	c.207G>A	p.E69E	Chr.2: 15942271-15942271 on Build GRCh38
6982143	c.188C>T	p.P63L	Chr.2: 15942252-15942252 on Build GRCh38
5609482	c.291C>T	p.F97F	Chr.2: 15942355-15942355 on Build GRCh38
1167728	c.365delC	p.R123fs*8	Chr.2: 15942429-15942429 on Build GRCh38
1216098	c.190A>G	p.S64G	Chr.2: 15942254-15942254 on Build GRCh38
4598943	c.383G>A	p.R128H	Chr.2: 15942447-15942447 on Build GRCh38
6951637	c.360C>A	p.F120L	Chr.2: 15942424-15942424 on Build GRCh38
6952581	c.280G>A	p.E94K	Chr.2: 15942344-15942344 on Build GRCh38
5806828	c.382C>T	p.R128C	Chr.2: 15942446-15942446 on Build GRCh38
4704459	c.385G>A	p.A129T	Chr.2: 15942449-15942449 on Build GRCh38
6970231	c.340G>A	p.D114N	Chr.2: 15942404-15942404 on Build GRCh38
6718938	c.169C>T	p.P57S	Chr.2: 15942233-15942233 on Build GRCh38
6971788	c.263G>T	p.W88L	Chr.2: 15942327-15942327 on Build GRCh38
6942375	c.203C>G	p.A68G	Chr.2: 15942267-15942267 on Build GRCh38
4437981	c.266G>A	p.G89D	Chr.2: 15942330-15942330 on Build GRCh38
6718941	c.311G>A	p.G104D	Chr.2: 15942375-15942375 on Build GRCh38
6942593	c.141G>T	p.E47D	Chr.2: 15942205-15942205 on Build GRCh38
2157145	c.173C>T	p.T58M	Chr.2: 15942237-15942237 on Build GRCh38
7293452	c.204G>A	p.A68A	Chr.2: 15942268-15942268 on Build GRCh38
4887736	c.180G>A	p.P60P	Chr.2: 15942244-15942244 on Build GRCh38
7340272	c.326C>T	p.P109L	Chr.2: 15942390-15942390 on Build GRCh38
4085917	c.267C>A	p.G89G	Chr.2: 15942331-15942331 on Build GRCh38
6965896	c.163C>A	p.L55M	Chr.2: 15942227-15942227 on Build GRCh38
24294	c.221C>T	p.P74L	Chr.2: 15942285-15942285 on Build GRCh38
6927981	c.250G>C	p.E84Q	Chr.2: 15942314-15942314 on Build GRCh38
6566780	c.230G>A	p.W77*	Chr.2: 15942294-15942294 on Build GRCh38
245849	c.296T>C	p.L99P	Chr.2: 15942360-15942360 on Build GRCh38
3300545	c.186G>A	p.S62S	Chr.2: 15942250-15942250 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs771914958	Chr.2: 15942447-15942447 on Build GRCh38
rs573377492	Chr.2: 15942253-15942253 on Build GRCh38
rs750717149	Chr.2: 15942291-15942291 on Build GRCh38
rs780448923	Chr.2: 15942387-15942387 on Build GRCh38
rs754869267	Chr.2: 15942255-15942255 on Build GRCh38
rs886796492	Chr.2: 15942451-15942451 on Build GRCh38
rs996755231	Chr.2: 15942382-15942382 on Build GRCh38
rs761787091	Chr.2: 15942375-15942375 on Build GRCh38
rs751463329	Chr.2: 15942254-15942254 on Build GRCh38
rs773995882	Chr.2: 15942434-15942434 on Build GRCh38
rs780606114	Chr.2: 15942301-15942301 on Build GRCh38
rs764741267	Chr.2: 15942230-15942230 on Build GRCh38
rs747413221	Chr.2: 15942307-15942307 on Build GRCh38
rs748818541	Chr.2: 15942424-15942424 on Build GRCh38
rs769152073	Chr.2: 15942420-15942420 on Build GRCh38
rs541917011	Chr.2: 15942227-15942227 on Build GRCh38
rs911937395	Chr.2: 15942286-15942286 on Build GRCh38
rs772981756	Chr.2: 15942235-15942235 on Build GRCh38
rs777292565	Chr.2: 15942423-15942423 on Build GRCh38
rs748734356	Chr.2: 15942418-15942418 on Build GRCh38
rs758657333	Chr.2: 15942383-15942383 on Build GRCh38
rs865923398	Chr.2: 15942250-15942250 on Build GRCh38
rs767463815	Chr.2: 15942266-15942266 on Build GRCh38
rs751789215	Chr.2: 15942261-15942290 on Build GRCh38
rs759320806	Chr.2: 15942440-15942440 on Build GRCh38
rs769240539	Chr.2: 15942308-15942308 on Build GRCh38
rs1048338754	Chr.2: 15942439-15942439 on Build GRCh38
rs121913667	Chr.2: 15942295-15942295 on Build GRCh38
rs540489428	Chr.2: 15942438-15942438 on Build GRCh38
rs762639151	Chr.2: 15942245-15942245 on Build GRCh38
rs781535490	Chr.2: 15942403-15942403 on Build GRCh38
rs751918450	Chr.2: 15942397-15942397 on Build GRCh38
rs747547602	Chr.2: 15942319-15942319 on Build GRCh38
rs759339159	Chr.2: 15942356-15942356 on Build GRCh38
rs148975024	Chr.2: 15942310-15942310 on Build GRCh38
rs921199233	Chr.2: 15942392-15942392 on Build GRCh38
rs750579922	Chr.2: 15942380-15942380 on Build GRCh38
rs767373881	Chr.2: 15942359-15942359 on Build GRCh38
rs963929622	Chr.2: 15942364-15942364 on Build GRCh38
rs151113760	Chr.2: 15942343-15942343 on Build GRCh38
rs113994115	Chr.2: 15942281-15942281 on Build GRCh38
rs1052552775	Chr.2: 15942269-15942269 on Build GRCh38
rs41264199	Chr.2: 15942271-15942271 on Build GRCh38
rs779000620	Chr.2: 15942288-15942288 on Build GRCh38
rs774081987	Chr.2: 15942347-15942347 on Build GRCh38
rs769401203	Chr.2: 15942322-15942322 on Build GRCh38
rs770512842	Chr.2: 15942433-15942433 on Build GRCh38
rs757360369	Chr.2: 15942285-15942285 on Build GRCh38
rs755400695	Chr.2: 15942398-15942398 on Build GRCh38
rs752749374	Chr.2: 15942366-15942366 on Build GRCh38
rs772714029	Chr.2: 15942334-15942334 on Build GRCh38

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