Product Details

Primer Sequences

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Primer Chromosome Location

Chr.2: 1839222-1839453 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

MYT1L

Entrez Gene ID

23040

Gene Name

myelin transcription factor 1 like

Gene Aliases

MRD39, NZF1, ZC2H2C2, ZC2HC4B

UniGene

Hs.434418

Gene Chromosome Location

Chr.2: 1789113-2331388 on Build GRCh38

Transcripts

NM_001303052.1 NM_015025.3 XM_011510318.1 XM_011510319.1 XM_011510320.2 XM_011510321.2 XM_011510322.2 XM_011510323.1 XM_011510324.1 XM_011510325.1 XM_011510326.1 XM_011510327.1 XM_011510328.2 XM_017003604.1 XM_017003605.1 XM_017003606.1 XM_017003607.1 XM_017003608.1 XM_017003609.1 XM_017003610.1 XM_017003611.1 XM_017003612.1 XM_017003613.1 XM_017003614.1 XM_017003615.1 XM_017003616.1 XM_017003617.1 XM_017003618.1 XM_017003619.1 XM_017003620.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
4774539	c.2958A>C	p.K986N	Chr.2: 1839271-1839271 on Build GRCh38
3575027	c.2981C>T	p.S994F	Chr.2: 1839242-1839242 on Build GRCh38
2711003	c.2942C>A	p.A981E	Chr.2: 1839287-1839287 on Build GRCh38
4411815	c.2998G>T	p.V1000F	Chr.2: 1839231-1839231 on Build GRCh38
4540685	c.2886G>A	p.Q962Q	Chr.2: 1839343-1839343 on Build GRCh38
6156387	c.2868G>T	p.G956G	Chr.2: 1839355-1839355 on Build GRCh38
7246023	c.3005C>A	p.T1002K	Chr.2: 1839224-1839224 on Build GRCh38
4411814	c.2992G>T	p.V998F	Chr.2: 1839231-1839231 on Build GRCh38
3971913	c.2916C>T	p.S972S	Chr.2: 1839307-1839307 on Build GRCh38
5445563	c.2999T>A	p.V1000D	Chr.2: 1839230-1839230 on Build GRCh38
4784093	c.2937G>A	p.A979A	Chr.2: 1839286-1839286 on Build GRCh38
6721268	c.2937_2938insC	p.A981fs*82	Chr.2: 1839291-1839292 on Build GRCh38
4307650	c.2903C>T	p.A968V	Chr.2: 1839320-1839320 on Build GRCh38
4404404	c.3001G>A	p.E1001K	Chr.2: 1839222-1839222 on Build GRCh38
5058504	c.2883C>T	p.G961G	Chr.2: 1839340-1839340 on Build GRCh38
5696564	c.2916C>A	p.S972R	Chr.2: 1839307-1839307 on Build GRCh38
1403777	c.2922C>T	p.S974S	Chr.2: 1839307-1839307 on Build GRCh38
5509784	c.2955C>T	p.D985D	Chr.2: 1839268-1839268 on Build GRCh38
4705295	c.2910G>A	p.A970A	Chr.2: 1839319-1839319 on Build GRCh38
4813874	c.2943G>C	p.K981N	Chr.2: 1839280-1839280 on Build GRCh38
3379958	c.2931C>A	p.P977P	Chr.2: 1839292-1839292 on Build GRCh38
6721267	c.2931_2932insC	p.A979fs*82	Chr.2: 1839291-1839292 on Build GRCh38
3695144	c.2951G>A	p.R984K	Chr.2: 1839278-1839278 on Build GRCh38
4485203	c.2906C>T	p.S969F	Chr.2: 1839317-1839317 on Build GRCh38
3695143	c.2945G>A	p.R982K	Chr.2: 1839278-1839278 on Build GRCh38
719000	c.2877C>A	p.C959*	Chr.2: 1839352-1839352 on Build GRCh38
6156388	c.2874G>T	p.G958G	Chr.2: 1839355-1839355 on Build GRCh38
4705292	c.2960A>G	p.Y987C	Chr.2: 1839263-1839263 on Build GRCh38
3575028	c.2987C>T	p.S996F	Chr.2: 1839242-1839242 on Build GRCh38
3575025	c.3000G>A	p.T1000T	Chr.2: 1839223-1839223 on Build GRCh38
5696565	c.2922C>A	p.S974R	Chr.2: 1839307-1839307 on Build GRCh38
3575029	c.2895G>A	p.G965G	Chr.2: 1839328-1839328 on Build GRCh38
283086	c.2927C>T	p.S976F	Chr.2: 1839302-1839302 on Build GRCh38
441941	c.2949G>C	p.K983N	Chr.2: 1839280-1839280 on Build GRCh38
1258637	c.3005C>T	p.T1002M	Chr.2: 1839224-1839224 on Build GRCh38
2711001	c.2962G>A	p.G988R	Chr.2: 1839267-1839267 on Build GRCh38
5631289	c.2917G>A	p.A973T	Chr.2: 1839306-1839306 on Build GRCh38
5509785	c.2961C>T	p.D987D	Chr.2: 1839268-1839268 on Build GRCh38
262281	c.2990G>T	p.W997L	Chr.2: 1839239-1839239 on Build GRCh38
269681	c.2909C>T	p.A970V	Chr.2: 1839320-1839320 on Build GRCh38
3962056	c.2881G>T	p.G961C	Chr.2: 1839348-1839348 on Build GRCh38
7246022	c.2999C>A	p.T1000K	Chr.2: 1839224-1839224 on Build GRCh38
1216548	c.2911T>C	p.S971P	Chr.2: 1839318-1839318 on Build GRCh38
4307648	c.2936C>A	p.A979E	Chr.2: 1839287-1839287 on Build GRCh38
6721257	c.2929G>A	p.G977R	Chr.2: 1839300-1839300 on Build GRCh38
4485204	c.2912C>T	p.S971F	Chr.2: 1839317-1839317 on Build GRCh38
4307651	c.2902G>A	p.A968T	Chr.2: 1839321-1839321 on Build GRCh38
3379959	c.2937C>A	p.P979P	Chr.2: 1839292-1839292 on Build GRCh38
4705293	c.2966A>G	p.Y989C	Chr.2: 1839263-1839263 on Build GRCh38
1403776	c.2943G>A	p.A981A	Chr.2: 1839286-1839286 on Build GRCh38
4774538	c.2952A>C	p.K984N	Chr.2: 1839271-1839271 on Build GRCh38
3962055	c.2875G>T	p.G959C	Chr.2: 1839348-1839348 on Build GRCh38
4307646	c.2956G>A	p.G986R	Chr.2: 1839267-1839267 on Build GRCh38
1013718	c.3007G>A	p.E1003K	Chr.2: 1839222-1839222 on Build GRCh38
4862193	c.2871C>A	p.C957*	Chr.2: 1839352-1839352 on Build GRCh38
1733677	c.2861G>T	p.C954F	Chr.2: 1839368-1839368 on Build GRCh38
4540684	c.2880G>A	p.Q960Q	Chr.2: 1839343-1839343 on Build GRCh38
5058505	c.2889C>T	p.G963G	Chr.2: 1839340-1839340 on Build GRCh38
3575030	c.2901G>A	p.G967G	Chr.2: 1839328-1839328 on Build GRCh38
6721256	c.2923G>A	p.G975R	Chr.2: 1839300-1839300 on Build GRCh38
2711004	c.2908G>A	p.A970T	Chr.2: 1839321-1839321 on Build GRCh38
4705294	c.2904G>A	p.A968A	Chr.2: 1839319-1839319 on Build GRCh38
5445562	c.2993T>A	p.V998D	Chr.2: 1839230-1839230 on Build GRCh38
6721248	c.2999C>T	p.T1000M	Chr.2: 1839224-1839224 on Build GRCh38
1291388	c.2923G>A	p.A975T	Chr.2: 1839306-1839306 on Build GRCh38
3575026	c.3006G>A	p.T1002T	Chr.2: 1839223-1839223 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs745509665	Chr.2: 1839319-1839319 on Build GRCh38
rs373901652	Chr.2: 1839321-1839321 on Build GRCh38
rs767499945	Chr.2: 1839412-1839412 on Build GRCh38
rs768069026	Chr.2: 1839343-1839343 on Build GRCh38
rs372435818	Chr.2: 1839413-1839413 on Build GRCh38
rs755045694	Chr.2: 1839407-1839407 on Build GRCh38
rs766663726	Chr.2: 1839387-1839387 on Build GRCh38
rs200125635	Chr.2: 1839307-1839307 on Build GRCh38
rs779983229	Chr.2: 1839267-1839267 on Build GRCh38
rs755973131	Chr.2: 1839286-1839286 on Build GRCh38
rs773769801	Chr.2: 1839364-1839364 on Build GRCh38
rs888872136	Chr.2: 1839244-1839244 on Build GRCh38
rs777718481	Chr.2: 1839301-1839301 on Build GRCh38
rs778693756	Chr.2: 1839316-1839316 on Build GRCh38
rs541692429	Chr.2: 1839392-1839392 on Build GRCh38
rs762215015	Chr.2: 1839259-1839259 on Build GRCh38
rs571062392	Chr.2: 1839322-1839322 on Build GRCh38
rs942823146	Chr.2: 1839268-1839268 on Build GRCh38
rs573219610	Chr.2: 1839422-1839422 on Build GRCh38
rs750861804	Chr.2: 1839344-1839344 on Build GRCh38
rs749215430	Chr.2: 1839306-1839306 on Build GRCh38
rs763261790	Chr.2: 1839378-1839378 on Build GRCh38
rs757246743	Chr.2: 1839415-1839415 on Build GRCh38
rs1022482889	Chr.2: 1839363-1839363 on Build GRCh38
rs751569491	Chr.2: 1839400-1839400 on Build GRCh38
rs1052642314	Chr.2: 1839334-1839334 on Build GRCh38
rs762411264	Chr.2: 1839351-1839351 on Build GRCh38
rs62114684	Chr.2: 1839304-1839304 on Build GRCh38
rs59128763	Chr.2: 1839358-1839358 on Build GRCh38
rs758706264	Chr.2: 1839263-1839263 on Build GRCh38
rs756501070	Chr.2: 1839349-1839349 on Build GRCh38
rs754127474	Chr.2: 1839255-1839255 on Build GRCh38
rs760284404	Chr.2: 1839325-1839325 on Build GRCh38
rs778677295	Chr.2: 1839417-1839417 on Build GRCh38
rs909954796	Chr.2: 1839257-1839257 on Build GRCh38
rs751728106	Chr.2: 1839277-1839277 on Build GRCh38

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