Product Details

Primer Sequences

Log in to view

Primer Chromosome Location

Chr.1: 20807318-20807543 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

EIF4G3

Entrez Gene ID

8672

Gene Name

eukaryotic translation initiation factor 4 gamma 3

Gene Aliases

eIF-4G 3, eIF4G 3, eIF4GII

UniGene

Hs.467084

Gene Chromosome Location

Chr.1: 20806292-21177320 on Build GRCh38

Transcripts

NM_001198801.1 NM_001198802.1 NM_003760.4 XM_011542356.2 XM_011542361.2 XM_011542370.1 XM_011542371.1 XM_011542374.1 XM_011542375.2 XM_011542381.2 XM_017002672.1 XM_017002673.1 XM_017002674.1 XM_017002675.1 XM_017002676.1 XM_017002677.1 XM_017002678.1 XM_017002679.1 XM_017002680.1 XM_017002681.1 XM_017002682.1 XM_017002683.1 XM_017002684.1 XM_017002685.1 XM_017002686.1 XM_017002687.1 XM_017002688.1 XM_017002689.1 XM_017002690.1 XM_017002691.1 XM_017002692.1 XM_017002693.1 XM_017002694.1 XM_017002695.1 XM_017002696.1 XM_017002697.1 XM_017002698.1 XM_017002699.1 XM_017002700.1 XM_017002701.1 XM_017002702.1 XM_017002703.1 XM_017002704.1 XM_017002705.1 XM_017002706.1 XM_017002707.1 XM_017002708.1 XM_017002709.1

Cosmic Detail

View Less

Cosmic ID	Mutation	AA	Transcript Location
5025201	c.4682C>A	p.P1561H	Chr.1: 20807413-20807413 on Build GRCh38
6323387	c.3082G>A	p.E1028K	Chr.1: 20807465-20807465 on Build GRCh38
7136417	c.4722C>A	p.V1574V	Chr.1: 20807373-20807373 on Build GRCh38
463884	c.4703G>A	p.G1568D	Chr.1: 20807392-20807392 on Build GRCh38
6653029	c.3189G>A	p.T1063T	Chr.1: 20807358-20807358 on Build GRCh38
6996471	c.4685G>T	p.G1562V	Chr.1: 20807392-20807392 on Build GRCh38
6652998	c.4644C>T	p.S1548S	Chr.1: 20807451-20807451 on Build GRCh38
463885	c.4685G>A	p.G1562D	Chr.1: 20807392-20807392 on Build GRCh38
5025202	c.4664C>A	p.P1555H	Chr.1: 20807413-20807413 on Build GRCh38
678743	c.4676A>G	p.K1559R	Chr.1: 20807419-20807419 on Build GRCh38
5590739	c.4718C>T	p.S1573F	Chr.1: 20807377-20807377 on Build GRCh38
6652997	c.3097G>A	p.E1033K	Chr.1: 20807450-20807450 on Build GRCh38
6507035	c.4680G>T	p.G1560G	Chr.1: 20807397-20807397 on Build GRCh38
6540167	c.4767G>A	p.E1589E	Chr.1: 20807328-20807328 on Build GRCh38
6996470	c.4703G>T	p.G1568V	Chr.1: 20807392-20807392 on Build GRCh38
7136419	c.3174C>A	p.V1058V	Chr.1: 20807373-20807373 on Build GRCh38
5590740	c.4700C>T	p.S1567F	Chr.1: 20807377-20807377 on Build GRCh38
6540168	c.4749G>A	p.E1583E	Chr.1: 20807328-20807328 on Build GRCh38
903454	c.4661A>C	p.K1554T	Chr.1: 20807434-20807434 on Build GRCh38
678744	c.4658A>G	p.K1553R	Chr.1: 20807419-20807419 on Build GRCh38
5590741	c.3170C>T	p.S1057F	Chr.1: 20807377-20807377 on Build GRCh38
6540169	c.3219G>A	p.E1073E	Chr.1: 20807328-20807328 on Build GRCh38
3726770	c.4673A>G	p.Q1558R	Chr.1: 20807404-20807404 on Build GRCh38
6653031	c.4686C>T	p.G1562G	Chr.1: 20807391-20807391 on Build GRCh38
6507034	c.4698G>T	p.G1566G	Chr.1: 20807397-20807397 on Build GRCh38
3705463	c.4692G>A	p.Q1564Q	Chr.1: 20807403-20807403 on Build GRCh38
6323385	c.4630G>A	p.E1544K	Chr.1: 20807465-20807465 on Build GRCh38
6652996	c.4627G>A	p.E1543K	Chr.1: 20807450-20807450 on Build GRCh38
6996472	c.3155G>T	p.G1052V	Chr.1: 20807392-20807392 on Build GRCh38
3726769	c.4691A>G	p.Q1564R	Chr.1: 20807404-20807404 on Build GRCh38
6653030	c.4704C>T	p.G1568G	Chr.1: 20807391-20807391 on Build GRCh38
6323386	c.4612G>A	p.E1538K	Chr.1: 20807465-20807465 on Build GRCh38
6507036	c.3150G>T	p.G1050G	Chr.1: 20807397-20807397 on Build GRCh38
3705464	c.4674G>A	p.Q1558Q	Chr.1: 20807403-20807403 on Build GRCh38
6653032	c.3156C>T	p.G1052G	Chr.1: 20807391-20807391 on Build GRCh38
6652995	c.4645G>A	p.E1549K	Chr.1: 20807450-20807450 on Build GRCh38
3966239	c.4708G>A	p.A1570T	Chr.1: 20807369-20807369 on Build GRCh38
903455	c.4643A>C	p.K1548T	Chr.1: 20807434-20807434 on Build GRCh38
6653000	c.3096C>T	p.S1032S	Chr.1: 20807451-20807451 on Build GRCh38
4927052	c.4747G>A	p.E1583K	Chr.1: 20807348-20807348 on Build GRCh38
4927053	c.4729G>A	p.E1577K	Chr.1: 20807348-20807348 on Build GRCh38
3966238	c.4726G>A	p.A1576T	Chr.1: 20807369-20807369 on Build GRCh38
5596647	c.3134C>A	p.P1045H	Chr.1: 20807413-20807413 on Build GRCh38
6653028	c.4719G>A	p.T1573T	Chr.1: 20807358-20807358 on Build GRCh38
6653053	c.4629C>T	p.D1543D	Chr.1: 20807466-20807466 on Build GRCh38
6653054	c.4611C>T	p.D1537D	Chr.1: 20807466-20807466 on Build GRCh38
6652999	c.4626C>T	p.S1542S	Chr.1: 20807451-20807451 on Build GRCh38
7136418	c.4704C>A	p.V1568V	Chr.1: 20807373-20807373 on Build GRCh38
6653055	c.3081C>T	p.D1027D	Chr.1: 20807466-20807466 on Build GRCh38
6653027	c.4737G>A	p.T1579T	Chr.1: 20807358-20807358 on Build GRCh38

View More

SNP Detail

SNP ID	Chromosome Location
rs867114309	Chr.1: 20807369-20807369 on Build GRCh38
rs747687791	Chr.1: 20807505-20807507 on Build GRCh38
rs772236365	Chr.1: 20807417-20807417 on Build GRCh38
rs749034314	Chr.1: 20807359-20807359 on Build GRCh38
rs762356088	Chr.1: 20807371-20807371 on Build GRCh38
rs746060850	Chr.1: 20807383-20807383 on Build GRCh38
rs759165740	Chr.1: 20807472-20807472 on Build GRCh38
rs573551412	Chr.1: 20807430-20807430 on Build GRCh38
rs775631377	Chr.1: 20807418-20807418 on Build GRCh38
rs11584562	Chr.1: 20807403-20807403 on Build GRCh38
rs866320837	Chr.1: 20807377-20807377 on Build GRCh38
rs200368420	Chr.1: 20807406-20807406 on Build GRCh38
rs1037917085	Chr.1: 20807486-20807486 on Build GRCh38
rs765620407	Chr.1: 20807460-20807460 on Build GRCh38
rs146742995	Chr.1: 20807451-20807451 on Build GRCh38
rs770874174	Chr.1: 20807370-20807370 on Build GRCh38
rs371347072	Chr.1: 20807390-20807390 on Build GRCh38
rs540921938	Chr.1: 20807466-20807466 on Build GRCh38
rs762113871	Chr.1: 20807457-20807457 on Build GRCh38
rs767142331	Chr.1: 20807498-20807498 on Build GRCh38
rs769137304	Chr.1: 20807447-20807447 on Build GRCh38

View Full Product Details