Product Details

Primer Sequences

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Primer Chromosome Location

Chr.19: 36626194-36626433 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

ZNF382

Entrez Gene ID

84911

Gene Name

zinc finger protein 382

Gene Aliases

KS1

UniGene

Hs.631591

Gene Chromosome Location

Chr.19: 36605305-36628597 on Build GRCh38

Transcripts

NM_001256838.1 NM_032825.4

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6829720	c.480G>T	p.K160N	Chr.19: 36626377-36626377 on Build GRCh38
6829723	c.494G>A	p.G165E	Chr.19: 36626394-36626394 on Build GRCh38
4077401	c.323T>G	p.L108R	Chr.19: 36626223-36626223 on Build GRCh38
5144815	c.372G>T	p.K124N	Chr.19: 36626272-36626272 on Build GRCh38
6879984	c.421A>T	p.K141*	Chr.19: 36626318-36626318 on Build GRCh38
6465717	c.432A>C	p.K144N	Chr.19: 36626329-36626329 on Build GRCh38
7399031	c.380G>T	p.R127L	Chr.19: 36626277-36626277 on Build GRCh38
6524918	c.414T>A	p.P138P	Chr.19: 36626311-36626311 on Build GRCh38
4077400	c.326T>G	p.L109R	Chr.19: 36626223-36626223 on Build GRCh38
1233960	c.504G>T	p.E168D	Chr.19: 36626401-36626401 on Build GRCh38
1393104	c.338G>T	p.R113I	Chr.19: 36626235-36626235 on Build GRCh38
3756690	c.503A>G	p.E168G	Chr.19: 36626400-36626400 on Build GRCh38
7149170	c.516C>T	p.L172L	Chr.19: 36626413-36626413 on Build GRCh38
3756691	c.500A>G	p.E167G	Chr.19: 36626400-36626400 on Build GRCh38
3199807	c.425T>A	p.V142D	Chr.19: 36626322-36626322 on Build GRCh38
6465718	c.429A>C	p.K143N	Chr.19: 36626329-36626329 on Build GRCh38
3199813	c.522C>G	p.T174T	Chr.19: 36626419-36626419 on Build GRCh38
7077016	c.299C>A	p.P100H	Chr.19: 36626196-36626196 on Build GRCh38
6084443	c.460A>G	p.S154G	Chr.19: 36626360-36626360 on Build GRCh38
7096466	c.455G>C	p.R152T	Chr.19: 36626352-36626352 on Build GRCh38
5435524	c.341A>C	p.N114T	Chr.19: 36626241-36626241 on Build GRCh38
7112817	c.464C>A	p.P155H	Chr.19: 36626364-36626364 on Build GRCh38
5367970	c.318_319insA	p.L109fs*3	Chr.19: 36626215-36626216 on Build GRCh38
4486753	c.309C>T	p.F103F	Chr.19: 36626206-36626206 on Build GRCh38
1304476	c.467C>A	p.P156H	Chr.19: 36626364-36626364 on Build GRCh38
6150355	c.485G>C	p.G162A	Chr.19: 36626382-36626382 on Build GRCh38
4077399	c.321A>C	p.K107N	Chr.19: 36626221-36626221 on Build GRCh38
5144814	c.335G>T	p.R112I	Chr.19: 36626235-36626235 on Build GRCh38
4077403	c.364C>A	p.L122I	Chr.19: 36626264-36626264 on Build GRCh38
6829722	c.497G>A	p.G166E	Chr.19: 36626394-36626394 on Build GRCh38
4486754	c.306C>T	p.F102F	Chr.19: 36626206-36626206 on Build GRCh38
6879985	c.418A>T	p.K140*	Chr.19: 36626318-36626318 on Build GRCh38
7077017	c.296C>A	p.P99H	Chr.19: 36626196-36626196 on Build GRCh38
1271334	c.479A>C	p.K160T	Chr.19: 36626376-36626376 on Build GRCh38
6437368	c.312C>G	p.I104M	Chr.19: 36626209-36626209 on Build GRCh38
4077398	c.324A>C	p.K108N	Chr.19: 36626221-36626221 on Build GRCh38
6524919	c.411T>A	p.P137P	Chr.19: 36626311-36626311 on Build GRCh38
7399032	c.377G>T	p.R126L	Chr.19: 36626277-36626277 on Build GRCh38
4077402	c.367C>A	p.L123I	Chr.19: 36626264-36626264 on Build GRCh38
4336521	c.427delA	p.N144fs*5	Chr.19: 36626327-36626327 on Build GRCh38
6829721	c.477G>T	p.K159N	Chr.19: 36626377-36626377 on Build GRCh38
4282075	c.422T>A	p.V141D	Chr.19: 36626322-36626322 on Build GRCh38
1393105	c.375G>T	p.K125N	Chr.19: 36626272-36626272 on Build GRCh38
3199808	c.430delA	p.N145fs*5	Chr.19: 36626327-36626327 on Build GRCh38
7323973	c.476A>C	p.K159T	Chr.19: 36626376-36626376 on Build GRCh38
6437369	c.309C>G	p.I103M	Chr.19: 36626209-36626209 on Build GRCh38
3822820	c.519C>G	p.T173T	Chr.19: 36626419-36626419 on Build GRCh38
286847	c.380G>A	p.R127H	Chr.19: 36626277-36626277 on Build GRCh38
7096467	c.452G>C	p.R151T	Chr.19: 36626352-36626352 on Build GRCh38
5367971	c.315_316insA	p.L108fs*3	Chr.19: 36626215-36626216 on Build GRCh38
6084442	c.463A>G	p.S155G	Chr.19: 36626360-36626360 on Build GRCh38
6150356	c.482G>C	p.G161A	Chr.19: 36626382-36626382 on Build GRCh38
7149171	c.513C>T	p.L171L	Chr.19: 36626413-36626413 on Build GRCh38
5435523	c.344A>C	p.N115T	Chr.19: 36626241-36626241 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs3108171	Chr.19: 36626400-36626400 on Build GRCh38
rs772050971	Chr.19: 36626234-36626234 on Build GRCh38
rs781264235	Chr.19: 36626386-36626386 on Build GRCh38
rs778805731	Chr.19: 36626222-36626222 on Build GRCh38
rs763389271	Chr.19: 36626263-36626263 on Build GRCh38
rs754114549	Chr.19: 36626348-36626348 on Build GRCh38
rs747949757	Chr.19: 36626361-36626361 on Build GRCh38
rs142570474	Chr.19: 36626277-36626277 on Build GRCh38
rs776464213	Chr.19: 36626262-36626262 on Build GRCh38
rs764611801	Chr.19: 36626276-36626276 on Build GRCh38
rs1032904837	Chr.19: 36626252-36626252 on Build GRCh38
rs768086756	Chr.19: 36626288-36626288 on Build GRCh38
rs778609516	Chr.19: 36626353-36626353 on Build GRCh38
rs772538250	Chr.19: 36626235-36626235 on Build GRCh38
rs777795980	Chr.19: 36626376-36626376 on Build GRCh38
rs770449856	Chr.19: 36626260-36626260 on Build GRCh38
rs533817629	Chr.19: 36626351-36626351 on Build GRCh38
rs760253473	Chr.19: 36626244-36626244 on Build GRCh38
rs552027724	Chr.19: 36626341-36626341 on Build GRCh38
rs757262971	Chr.19: 36626311-36626324 on Build GRCh38
rs750423107	Chr.19: 36626332-36626332 on Build GRCh38
rs766485216	Chr.19: 36626342-36626342 on Build GRCh38
rs748147772	Chr.19: 36626233-36626233 on Build GRCh38
rs758219017	Chr.19: 36626366-36626366 on Build GRCh38
rs566322984	Chr.19: 36626339-36626339 on Build GRCh38
rs762347609	Chr.19: 36626279-36626279 on Build GRCh38
rs747266278	Chr.19: 36626228-36626228 on Build GRCh38
rs746468500	Chr.19: 36626384-36626384 on Build GRCh38
rs181678050	Chr.19: 36626393-36626393 on Build GRCh38

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