Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.4: 86064174-86064677 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: MAPK10
Entrez Gene ID: 5602
Gene Name: mitogen-activated protein kinase 10
Gene Aliases: JNK3, JNK3A, PRKM10, SAPK1b, p493F12, p54bSAPK
UniGene: Hs.125503
Gene Chromosome Location: Chr.4: 86012296-86594117 on Build GRCh38
Transcripts: NM_001318067.1 NM_001318068.1 NM_001318069.1 NM_002753.4 NM_138980.3 NM_138982.3 XM_005263129.2 XM_005263130.2 XM_005263131.2 XM_005263135.3 XM_006714268.2 XM_006714269.2 XM_011532117.2 XM_011532118.2 XM_011532120.2 XM_011532121.2 XM_017008419.1 XM_017008420.1 XM_017008421.1 XM_017008422.1 XM_017008423.1 XM_017008424.1 XM_017008425.1 XM_017008426.1 XM_017008427.1 XM_017008428.1 XM_017008429.1 XM_017008430.1 XM_017008431.1 XM_017008432.1 XM_017008433.1 XM_017008434.1 XM_017008435.1 XM_017008436.1 XM_017008437.1 XM_017008438.1 XM_017008439.1 XM_017008440.1 XM_017008441.1 XM_017008442.1 XM_017008443.1 XM_017008444.1 XM_017008445.1 XM_017008446.1 XM_017008447.1 XM_017008448.1 XM_017008449.1 XM_017008450.1 XM_017008451.1 XM_017008452.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
481639	c.1110+1G>A	p.?	Chr.4: 86064265-86064265 on Build GRCh38
7336733	c.566A>G	p.D189G	Chr.4: 86064375-86064375 on Build GRCh38
375071	c.1080C>T	p.N360N	Chr.4: 86064296-86064296 on Build GRCh38
6469730	c.1098C>G	p.A366A	Chr.4: 86064278-86064278 on Build GRCh38
7336732	c.1001A>G	p.D334G	Chr.4: 86064375-86064375 on Build GRCh38
375072	c.645C>T	p.N215N	Chr.4: 86064296-86064296 on Build GRCh38
1058455	c.664G>A	p.E222K	Chr.4: 86064277-86064277 on Build GRCh38
1058457	c.619G>A	p.D207N	Chr.4: 86064322-86064322 on Build GRCh38
1058459	c.560C>T	p.A187V	Chr.4: 86064381-86064381 on Build GRCh38
5534265	c.565G>A	p.D189N	Chr.4: 86064376-86064376 on Build GRCh38
3606769	c.664G>T	p.E222*	Chr.4: 86064277-86064277 on Build GRCh38
481640	c.675+1G>A	p.?	Chr.4: 86064265-86064265 on Build GRCh38
3606771	c.662C>T	p.A221V	Chr.4: 86064279-86064279 on Build GRCh38
3606768	c.1099G>T	p.E367*	Chr.4: 86064277-86064277 on Build GRCh38
6707750	c.646G>A	p.V216I	Chr.4: 86064295-86064295 on Build GRCh38
3606770	c.1097C>T	p.A366V	Chr.4: 86064279-86064279 on Build GRCh38
6707749	c.1081G>A	p.V361I	Chr.4: 86064295-86064295 on Build GRCh38
6479100	c.663C>T	p.A221A	Chr.4: 86064278-86064278 on Build GRCh38
6707743	c.604_605insA	p.R202fs*18	Chr.4: 86064336-86064337 on Build GRCh38
1058456	c.1054G>A	p.D352N	Chr.4: 86064322-86064322 on Build GRCh38
6707742	c.1039_1040insA	p.R347fs*18	Chr.4: 86064336-86064337 on Build GRCh38
1058458	c.995C>T	p.A332V	Chr.4: 86064381-86064381 on Build GRCh38
5534264	c.1000G>A	p.D334N	Chr.4: 86064376-86064376 on Build GRCh38
6469731	c.663C>G	p.A221A	Chr.4: 86064278-86064278 on Build GRCh38
6479099	c.1098C>T	p.A366A	Chr.4: 86064278-86064278 on Build GRCh38
1058454	c.1099G>A	p.E367K	Chr.4: 86064277-86064277 on Build GRCh38

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