Product Details

Primer Sequences

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Primer Chromosome Location

Chr.11: 102229761-102229986 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

YAP1

Entrez Gene ID

10413

Gene Name

Yes associated protein 1

Gene Aliases

COB1, YAP, YAP2, YAP65, YKI

UniGene

Hs.503692

Gene Chromosome Location

Chr.11: 102109957-102233423 on Build GRCh38

Transcripts

NM_001130145.2 NM_001195044.1 NM_001195045.1 NM_001282097.1 NM_001282098.1 NM_001282099.1 NM_001282100.1 NM_001282101.1 NM_006106.4 XM_005271378.3 XM_005271380.3 XM_005271381.3 XM_005271383.3 XM_011542555.2 XM_011542556.2 XM_017017093.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6952281	c.1501C>A	p.L501I	Chr.11: 102229926-102229926 on Build GRCh38
5802533	c.1486delG	p.D496fs*>9	Chr.11: 102229911-102229911 on Build GRCh38
4165611	c.1477A>G	p.T493A	Chr.11: 102229902-102229902 on Build GRCh38
3985859	c.1237G>T	p.G413*	Chr.11: 102229824-102229824 on Build GRCh38
3791100	c.1248G>C	p.L416L	Chr.11: 102229835-102229835 on Build GRCh38
6479643	c.1402G>C	p.E468Q	Chr.11: 102229827-102229827 on Build GRCh38
6924419	c.1178C>A	p.A393D	Chr.11: 102229765-102229765 on Build GRCh38
1167854	c.1385_1386insA	p.M463fs*19	Chr.11: 102229810-102229811 on Build GRCh38
3791099	c.1410G>C	p.L470L	Chr.11: 102229835-102229835 on Build GRCh38
6930525	c.1395_1415del21	p.E466_P472delEGEELMP	Chr.11: 102229820-102229840 on Build GRCh38
6978432	c.1397A>T	p.E466V	Chr.11: 102229822-102229822 on Build GRCh38
3383142	c.1408C>A	p.L470M	Chr.11: 102229833-102229833 on Build GRCh38
6975199	c.1434G>T	p.L478F	Chr.11: 102229859-102229859 on Build GRCh38
6924418	c.1340C>A	p.A447D	Chr.11: 102229765-102229765 on Build GRCh38
6952282	c.1339C>A	p.L447I	Chr.11: 102229926-102229926 on Build GRCh38
5027475	c.1353G>C	p.*451Y	Chr.11: 102229940-102229940 on Build GRCh38
428285	c.1414C>T	p.P472S	Chr.11: 102229839-102229839 on Build GRCh38
1270628	c.1248G>A	p.L416L	Chr.11: 102229835-102229835 on Build GRCh38
6961931	c.1375G>A	p.E459K	Chr.11: 102229800-102229800 on Build GRCh38
3985858	c.1399G>T	p.G467*	Chr.11: 102229824-102229824 on Build GRCh38
5984662	c.1272G>C	p.L424F	Chr.11: 102229859-102229859 on Build GRCh38
6130605	c.1245G>A	p.E415E	Chr.11: 102229832-102229832 on Build GRCh38
3791101	c.1501C>T	p.L501F	Chr.11: 102229926-102229926 on Build GRCh38
1270627	c.1410G>A	p.L470L	Chr.11: 102229835-102229835 on Build GRCh38
5611207	c.1367G>A	p.G456E	Chr.11: 102229792-102229792 on Build GRCh38
6952279	c.1463C>A	p.S488Y	Chr.11: 102229888-102229888 on Build GRCh38
4165612	c.1315A>G	p.T439A	Chr.11: 102229902-102229902 on Build GRCh38
6930526	c.1233_1253del21	p.E412_P418delEGEELMP	Chr.11: 102229820-102229840 on Build GRCh38
6975200	c.1272G>T	p.L424F	Chr.11: 102229859-102229859 on Build GRCh38
3791102	c.1339C>T	p.L447F	Chr.11: 102229926-102229926 on Build GRCh38
6978433	c.1235A>T	p.E412V	Chr.11: 102229822-102229822 on Build GRCh38
5611208	c.1205G>A	p.G402E	Chr.11: 102229792-102229792 on Build GRCh38
6918553	c.1279G>C	p.D427H	Chr.11: 102229866-102229866 on Build GRCh38
5027474	c.1515G>C	p.*505Y	Chr.11: 102229940-102229940 on Build GRCh38
5802534	c.1324delG	p.D442fs*>9	Chr.11: 102229911-102229911 on Build GRCh38
6961932	c.1213G>A	p.E405K	Chr.11: 102229800-102229800 on Build GRCh38
6130604	c.1407G>A	p.E469E	Chr.11: 102229832-102229832 on Build GRCh38
2108109	c.1238G>C	p.G413A	Chr.11: 102229825-102229825 on Build GRCh38
3383143	c.1246C>A	p.L416M	Chr.11: 102229833-102229833 on Build GRCh38
2108108	c.1400G>C	p.G467A	Chr.11: 102229825-102229825 on Build GRCh38
5984661	c.1434G>C	p.L478F	Chr.11: 102229859-102229859 on Build GRCh38
4803269	c.1398A>G	p.E466E	Chr.11: 102229823-102229823 on Build GRCh38
6952280	c.1301C>A	p.S434Y	Chr.11: 102229888-102229888 on Build GRCh38
6479644	c.1240G>C	p.E414Q	Chr.11: 102229827-102229827 on Build GRCh38
466201	c.1432T>C	p.L478L	Chr.11: 102229857-102229857 on Build GRCh38
6918552	c.1441G>C	p.D481H	Chr.11: 102229866-102229866 on Build GRCh38
4803270	c.1236A>G	p.E412E	Chr.11: 102229823-102229823 on Build GRCh38
77040	c.1348T>A	p.L450I	Chr.11: 102229935-102229935 on Build GRCh38
1474942	c.1252C>T	p.P418S	Chr.11: 102229839-102229839 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs201772622	Chr.11: 102229818-102229818 on Build GRCh38
rs369837465	Chr.11: 102229952-102229952 on Build GRCh38
rs773457076	Chr.11: 102229785-102229785 on Build GRCh38
rs1022838674	Chr.11: 102229828-102229828 on Build GRCh38
rs112713899	Chr.11: 102229871-102229871 on Build GRCh38
rs779614719	Chr.11: 102229937-102229937 on Build GRCh38
rs759882394	Chr.11: 102229829-102229829 on Build GRCh38
rs754789933	Chr.11: 102229951-102229951 on Build GRCh38
rs756621827	Chr.11: 102229861-102229861 on Build GRCh38
rs758047587	Chr.11: 102229919-102229919 on Build GRCh38
rs769873665	Chr.11: 102229953-102229953 on Build GRCh38
rs749962892	Chr.11: 102229902-102229902 on Build GRCh38
rs534468390	Chr.11: 102229844-102229844 on Build GRCh38
rs148574447	Chr.11: 102229821-102229821 on Build GRCh38
rs746816956	Chr.11: 102229945-102229945 on Build GRCh38
rs766554722	Chr.11: 102229819-102229819 on Build GRCh38
rs759000569	Chr.11: 102229934-102229935 on Build GRCh38
rs141269128	Chr.11: 102229841-102229841 on Build GRCh38
rs764690657	Chr.11: 102229884-102229884 on Build GRCh38
rs956054285	Chr.11: 102229947-102229947 on Build GRCh38

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