Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.12: 31389221-31389468 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: DENND5B
Entrez Gene ID: 160518
Gene Name: DENN domain containing 5B
Gene Aliases: -
UniGene: Hs.118166
Gene Chromosome Location: Chr.12: 31382223-31591018 on Build GRCh38
Transcripts: NM_001308339.1 NM_144973.3 XM_005253326.2 XM_005253327.3 XM_005253330.3 XM_006719040.3 XM_011520590.2 XM_017018896.1 XM_017018897.1 XM_017018898.1 XM_017018899.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
6642512	c.3602A>C	p.K1201T	Chr.12: 31389363-31389363 on Build GRCh38
4813694	c.3724A>T	p.I1242F	Chr.12: 31389346-31389346 on Build GRCh38
6876503	c.3696G>A	p.R1232R	Chr.12: 31389374-31389374 on Build GRCh38
6136794	c.3605A>G	p.D1202G	Chr.12: 31389360-31389360 on Build GRCh38
4875523	c.3610C>A	p.L1204I	Chr.12: 31389460-31389460 on Build GRCh38
4206645	c.3636T>G	p.I1212M	Chr.12: 31389434-31389434 on Build GRCh38
4206644	c.3714C>T	p.G1238G	Chr.12: 31389356-31389356 on Build GRCh38
2205573	c.3531T>G	p.I1177M	Chr.12: 31389434-31389434 on Build GRCh38
6574454	c.3533A>T	p.Q1178L	Chr.12: 31389432-31389432 on Build GRCh38
2205572	c.3609C>T	p.G1203G	Chr.12: 31389356-31389356 on Build GRCh38
6642513	c.3707A>C	p.K1236T	Chr.12: 31389363-31389363 on Build GRCh38
4982948	c.3517G>C	p.D1173H	Chr.12: 31389448-31389448 on Build GRCh38
4961794	c.3629G>T	p.C1210F	Chr.12: 31389336-31389336 on Build GRCh38
6136795	c.3710A>G	p.D1237G	Chr.12: 31389360-31389360 on Build GRCh38
6025291	c.3568A>G	p.N1190D	Chr.12: 31389397-31389397 on Build GRCh38
693352	c.3532C>A	p.Q1178K	Chr.12: 31389433-31389433 on Build GRCh38
4428954	c.3630C>T	p.V1210V	Chr.12: 31389440-31389440 on Build GRCh38
6574455	c.3638A>T	p.Q1213L	Chr.12: 31389432-31389432 on Build GRCh38
4428953	c.3525C>T	p.V1175V	Chr.12: 31389440-31389440 on Build GRCh38
938737	c.3505C>A	p.L1169I	Chr.12: 31389460-31389460 on Build GRCh38
4862227	c.3637C>A	p.Q1213K	Chr.12: 31389433-31389433 on Build GRCh38
4982949	c.3622G>C	p.D1208H	Chr.12: 31389448-31389448 on Build GRCh38
86298	c.3598G>T	p.G1200W	Chr.12: 31389367-31389367 on Build GRCh38
6876502	c.3591G>A	p.R1197R	Chr.12: 31389374-31389374 on Build GRCh38
4961795	c.3734G>T	p.C1245F	Chr.12: 31389336-31389336 on Build GRCh38
222238	c.3578A>T	p.N1193I	Chr.12: 31389387-31389387 on Build GRCh38
431023	c.3619A>T	p.I1207F	Chr.12: 31389346-31389346 on Build GRCh38
6025292	c.3673A>G	p.N1225D	Chr.12: 31389397-31389397 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs774604276	Chr.12: 31389298-31389298 on Build GRCh38
rs139596083	Chr.12: 31389240-31389240 on Build GRCh38
rs763677427	Chr.12: 31389405-31389405 on Build GRCh38
rs752287397	Chr.12: 31389391-31389391 on Build GRCh38
rs545452374	Chr.12: 31389272-31389272 on Build GRCh38
rs776787002	Chr.12: 31389255-31389255 on Build GRCh38
rs932185335	Chr.12: 31389274-31389274 on Build GRCh38
rs781728489	Chr.12: 31389425-31389425 on Build GRCh38
rs751299333	Chr.12: 31389410-31389410 on Build GRCh38
rs75339388	Chr.12: 31389419-31389419 on Build GRCh38
rs1036947468	Chr.12: 31389292-31389292 on Build GRCh38
rs766226529	Chr.12: 31389319-31389319 on Build GRCh38
rs921427193	Chr.12: 31389394-31389394 on Build GRCh38
rs756967715	Chr.12: 31389414-31389414 on Build GRCh38
rs762901082	Chr.12: 31389278-31389278 on Build GRCh38
rs775643939	Chr.12: 31389275-31389275 on Build GRCh38
rs10843937	Chr.12: 31389257-31389257 on Build GRCh38
rs375729543	Chr.12: 31389401-31389401 on Build GRCh38
rs765021778	Chr.12: 31389370-31389370 on Build GRCh38
rs761990304	Chr.12: 31389309-31389309 on Build GRCh38
rs768943296	Chr.12: 31389296-31389296 on Build GRCh38
rs372710210	Chr.12: 31389356-31389356 on Build GRCh38
rs901112447	Chr.12: 31389306-31389306 on Build GRCh38
rs559061851	Chr.12: 31389334-31389334 on Build GRCh38

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