Product Details

Primer Sequences

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Primer Chromosome Location

Chr.10: 32919802-32920043 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

ITGB1

Entrez Gene ID

3688

Gene Name

integrin subunit beta 1

Gene Aliases

CD29, FNRB, GPIIA, MDF2, MSK12, VLA-BETA, VLAB

UniGene

Hs.643813

Gene Chromosome Location

Chr.10: 32900318-32958365 on Build GRCh38

Transcripts

NM_002211.3 NM_033668.2 NM_133376.2

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
917805	c.1433A>G	p.H478R	Chr.10: 32919921-32919921 on Build GRCh38
4693355	c.1469+1G>A	p.?	Chr.10: 32919884-32919884 on Build GRCh38
917809	c.1314G>T	p.K438N	Chr.10: 32920040-32920040 on Build GRCh38
917807	c.1334T>A	p.I445N	Chr.10: 32920020-32920020 on Build GRCh38
4875292	c.1433A>G	p.H478R	Chr.10: 32919921-32919921 on Build GRCh38
4868448	c.1314G>T	p.K438N	Chr.10: 32920040-32920040 on Build GRCh38
4013880	c.1461C>T	p.G487G	Chr.10: 32919893-32919893 on Build GRCh38
4013879	c.1461C>T	p.G487G	Chr.10: 32919893-32919893 on Build GRCh38
1560802	c.1313delA	p.K438fs*17	Chr.10: 32920041-32920041 on Build GRCh38
5077903	c.1313delA	p.K438fs*17	Chr.10: 32920041-32920041 on Build GRCh38
4013883	c.1352C>T	p.T451M	Chr.10: 32920002-32920002 on Build GRCh38
4013882	c.1352C>T	p.T451M	Chr.10: 32920002-32920002 on Build GRCh38
4885385	c.1342C>G	p.L448V	Chr.10: 32920012-32920012 on Build GRCh38
3985598	c.1416T>C	p.P472P	Chr.10: 32919938-32919938 on Build GRCh38
3985599	c.1416T>C	p.P472P	Chr.10: 32919938-32919938 on Build GRCh38
4879995	c.1341T>G	p.P447P	Chr.10: 32920013-32920013 on Build GRCh38
4693356	c.1469+1G>A	p.?	Chr.10: 32919884-32919884 on Build GRCh38
684451	c.1469G>A	p.R490K	Chr.10: 32919885-32919885 on Build GRCh38
348241	c.1412T>A	p.I471N	Chr.10: 32919942-32919942 on Build GRCh38
4442665	c.1409G>A	p.G470D	Chr.10: 32919945-32919945 on Build GRCh38
4885386	c.1342C>G	p.L448V	Chr.10: 32920012-32920012 on Build GRCh38
4442666	c.1409G>A	p.G470D	Chr.10: 32919945-32919945 on Build GRCh38
4879996	c.1341T>G	p.P447P	Chr.10: 32920013-32920013 on Build GRCh38
1646303	c.1469G>A	p.R490K	Chr.10: 32919885-32919885 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs377263167	Chr.10: 32919904-32919904 on Build GRCh38
rs201228879	Chr.10: 32920002-32920002 on Build GRCh38
rs754935937	Chr.10: 32919949-32919949 on Build GRCh38
rs543305169	Chr.10: 32919993-32919993 on Build GRCh38
rs201973516	Chr.10: 32919893-32919893 on Build GRCh38
rs775002495	Chr.10: 32919846-32919846 on Build GRCh38
rs201867204	Chr.10: 32919861-32919861 on Build GRCh38
rs778171708	Chr.10: 32919995-32919995 on Build GRCh38
rs111522124	Chr.10: 32919962-32919962 on Build GRCh38
rs765443724	Chr.10: 32919851-32919852 on Build GRCh38
rs199980084	Chr.10: 32919996-32919996 on Build GRCh38
rs771524178	Chr.10: 32919840-32919840 on Build GRCh38
rs749312525	Chr.10: 32920001-32920001 on Build GRCh38
rs759740155	Chr.10: 32919849-32919850 on Build GRCh38
rs1026236432	Chr.10: 32919849-32919849 on Build GRCh38
rs752504227	Chr.10: 32919854-32919854 on Build GRCh38
rs1009137692	Chr.10: 32919891-32919891 on Build GRCh38
rs202125974	Chr.10: 32919856-32919856 on Build GRCh38
rs955335980	Chr.10: 32919831-32919837 on Build GRCh38
rs151175196	Chr.10: 32919929-32919929 on Build GRCh38
rs199630291	Chr.10: 32919848-32919848 on Build GRCh38
rs201353503	Chr.10: 32919968-32919968 on Build GRCh38
rs758178134	Chr.10: 32919870-32919871 on Build GRCh38
rs761506383	Chr.10: 32919876-32919876 on Build GRCh38
rs753045262	Chr.10: 32919868-32919868 on Build GRCh38
rs180672316	Chr.10: 32919950-32919950 on Build GRCh38
rs143061769	Chr.10: 32919890-32919890 on Build GRCh38
rs749899655	Chr.10: 32919892-32919892 on Build GRCh38
rs974531843	Chr.10: 32919988-32919988 on Build GRCh38
rs199513073	Chr.10: 32919875-32919875 on Build GRCh38
rs756354856	Chr.10: 32919991-32919991 on Build GRCh38

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