Product Details

Primer Sequences

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Primer Chromosome Location

Chr.3: 70965862-70966029 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

FOXP1

Entrez Gene ID

27086

Gene Name

forkhead box P1

Gene Aliases

12CC4, HSPC215, MFH, QRF1, hFKH1B

UniGene

Hs.59368

Gene Chromosome Location

Chr.3: 70954714-71583989 on Build GRCh38

Transcripts

NM_001244808.1 NM_001244810.1 NM_001244812.1 NM_001244813.1 NM_001244814.1 NM_001244815.1 NM_001244816.1 NM_032682.5 XM_005264735.3 XM_005264736.3 XM_005264737.4 XM_005264742.3 XM_006713102.2 XM_006713103.2 XM_006713104.2 XM_011533584.2 XM_011533585.2 XM_011533588.2 XM_017006165.1 XM_017006166.1 XM_017006167.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
23406	c.1808G>A	p.R603Q	Chr.3: 70965971-70965971 on Build GRCh38
6582728	c.1748_1755delCTCTATAC	p.P583fs*34	Chr.3: 70966024-70966031 on Build GRCh38
5355033	c.1889+3_1889+11delGAGTATTGT	p.?	Chr.3: 70965879-70965887 on Build GRCh38
6098075	c.1812A>G	p.E604E	Chr.3: 70965967-70965967 on Build GRCh38
5418253	c.1750C>T	p.L584L	Chr.3: 70966029-70966029 on Build GRCh38
1048336	c.1832A>G	p.E611G	Chr.3: 70965947-70965947 on Build GRCh38
6666478	c.1848C>T	p.N616N	Chr.3: 70965931-70965931 on Build GRCh38
3597304	c.1876C>T	p.P626S	Chr.3: 70965903-70965903 on Build GRCh38
6946122	c.1856A>G	p.D619G	Chr.3: 70965923-70965923 on Build GRCh38
6933831	c.1783C>G	p.L595V	Chr.3: 70965996-70965996 on Build GRCh38
5865282	c.1807C>T	p.R603W	Chr.3: 70965972-70965972 on Build GRCh38
4975242	c.1857C>T	p.D619D	Chr.3: 70965922-70965922 on Build GRCh38
731643	c.1851G>A	p.E617E	Chr.3: 70965928-70965928 on Build GRCh38
5059940	c.1844G>A	p.S615N	Chr.3: 70965935-70965935 on Build GRCh38
4120075	c.1830G>T	p.M610I	Chr.3: 70965949-70965949 on Build GRCh38
4120074	c.1849G>A	p.E617K	Chr.3: 70965930-70965930 on Build GRCh38
6403257	c.1801G>A	p.A601T	Chr.3: 70965978-70965978 on Build GRCh38
6907229	c.1889+1G>A	p.?	Chr.3: 70965889-70965889 on Build GRCh38
4120076	c.1821C>T	p.N607N	Chr.3: 70965958-70965958 on Build GRCh38
350923	c.1871G>T	p.R624I	Chr.3: 70965908-70965908 on Build GRCh38
4834393	c.1810G>A	p.E604K	Chr.3: 70965969-70965969 on Build GRCh38
6964967	c.1772G>A	p.G591E	Chr.3: 70966007-70966007 on Build GRCh38
6219828	c.1810G>T	p.E604*	Chr.3: 70965969-70965969 on Build GRCh38
1048338	c.1800C>T	p.S600S	Chr.3: 70965979-70965979 on Build GRCh38
6939078	c.1760C>T	p.T587I	Chr.3: 70966019-70966019 on Build GRCh38
6939782	c.1888G>A	p.V630M	Chr.3: 70965891-70965891 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs748075031	Chr.3: 70965971-70965971 on Build GRCh38
rs749121207	Chr.3: 70965957-70965957 on Build GRCh38
rs754297044	Chr.3: 70965893-70965893 on Build GRCh38
rs771667463	Chr.3: 70965883-70965883 on Build GRCh38
rs754932182	Chr.3: 70965900-70965900 on Build GRCh38
rs766116383	Chr.3: 70965892-70965892 on Build GRCh38
rs772816590	Chr.3: 70965891-70965891 on Build GRCh38
rs761406403	Chr.3: 70965882-70965882 on Build GRCh38
rs778939994	Chr.3: 70965963-70965963 on Build GRCh38
rs369021347	Chr.3: 70965974-70965974 on Build GRCh38
rs753098583	Chr.3: 70965910-70965910 on Build GRCh38
rs751621278	Chr.3: 70965951-70965951 on Build GRCh38
rs373809702	Chr.3: 70965978-70965978 on Build GRCh38
rs147537388	Chr.3: 70965954-70965954 on Build GRCh38
rs757539300	Chr.3: 70965953-70965953 on Build GRCh38
rs770712857	Chr.3: 70965983-70965983 on Build GRCh38
rs768285337	Chr.3: 70965958-70965958 on Build GRCh38
rs777876809	Chr.3: 70965946-70965946 on Build GRCh38
rs759753513	Chr.3: 70965899-70965899 on Build GRCh38
rs758540752	Chr.3: 70965944-70965944 on Build GRCh38
rs970358469	Chr.3: 70965981-70965981 on Build GRCh38
rs760260048	Chr.3: 70965979-70965979 on Build GRCh38

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