Product Details

Primer Sequences

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Primer Chromosome Location

Chr.2: 99554374-99554513 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

AFF3

Entrez Gene ID

3899

Gene Name

AF4/FMR2 family member 3

Gene Aliases

LAF4, MLLT2-like

UniGene

Hs.444414

Gene Chromosome Location

Chr.2: 99545861-100142583 on Build GRCh38

Transcripts

NM_001025108.1 NM_002285.2 XM_005263943.3 XM_005263945.3 XM_011511169.2 XM_011511170.2 XM_011511171.2 XM_011511172.2 XM_011511173.2 XM_011511174.2 XM_011511175.2 XM_011511176.2 XM_011511177.2 XM_011511178.2 XM_011511179.2 XM_017004085.1 XM_017004086.1 XM_017004087.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
5991415	c.3546G>T	p.M1182I	Chr.2: 99554399-99554399 on Build GRCh38
5575612	c.3469T>C	p.S1157P	Chr.2: 99554476-99554476 on Build GRCh38
3396433	c.3497C>T	p.A1166V	Chr.2: 99554448-99554448 on Build GRCh38
715022	c.3533G>A	p.R1178H	Chr.2: 99554412-99554412 on Build GRCh38
6595895	c.3532C>T	p.R1178C	Chr.2: 99554413-99554413 on Build GRCh38
1004420	c.3490G>A	p.A1164T	Chr.2: 99554455-99554455 on Build GRCh38
715021	c.3501G>T	p.L1167L	Chr.2: 99554444-99554444 on Build GRCh38
5038287	c.3443A>C	p.N1148T	Chr.2: 99554502-99554502 on Build GRCh38
1004419	c.3548C>T	p.A1183V	Chr.2: 99554397-99554397 on Build GRCh38
335148	c.3489C>T	p.N1163N	Chr.2: 99554456-99554456 on Build GRCh38
5736149	c.3496G>A	p.A1166T	Chr.2: 99554449-99554449 on Build GRCh38
4083706	c.3507G>A	p.P1169P	Chr.2: 99554438-99554438 on Build GRCh38
4083705	c.3559G>A	p.V1187I	Chr.2: 99554386-99554386 on Build GRCh38
3564231	c.3503C>T	p.S1168F	Chr.2: 99554442-99554442 on Build GRCh38
3564230	c.3505C>T	p.P1169S	Chr.2: 99554440-99554440 on Build GRCh38
6244873	c.3504C>A	p.S1168S	Chr.2: 99554441-99554441 on Build GRCh38
3708764	c.3495C>A	p.S1165R	Chr.2: 99554450-99554450 on Build GRCh38
6595917	c.3529C>T	p.Q1177*	Chr.2: 99554416-99554416 on Build GRCh38
1481767	c.3506C>T	p.P1169L	Chr.2: 99554439-99554439 on Build GRCh38
3894362	c.3440C>T	p.P1147L	Chr.2: 99554505-99554505 on Build GRCh38
4660230	c.3454G>A	p.A1152T	Chr.2: 99554491-99554491 on Build GRCh38
6595916	c.3517G>A	p.V1173I	Chr.2: 99554428-99554428 on Build GRCh38
5393935	c.3486C>T	p.S1162S	Chr.2: 99554459-99554459 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs767846193	Chr.2: 99554406-99554406 on Build GRCh38
rs780887781	Chr.2: 99554456-99554456 on Build GRCh38
rs143764541	Chr.2: 99554482-99554482 on Build GRCh38
rs760851681	Chr.2: 99554492-99554492 on Build GRCh38
rs142364775	Chr.2: 99554410-99554410 on Build GRCh38
rs745505866	Chr.2: 99554458-99554458 on Build GRCh38
rs766758032	Chr.2: 99554412-99554412 on Build GRCh38
rs371101321	Chr.2: 99554471-99554471 on Build GRCh38
rs1015661536	Chr.2: 99554462-99554462 on Build GRCh38
rs773572168	Chr.2: 99554491-99554491 on Build GRCh38
rs200904404	Chr.2: 99554438-99554438 on Build GRCh38
rs765114515	Chr.2: 99554441-99554441 on Build GRCh38
rs376932214	Chr.2: 99554451-99554451 on Build GRCh38
rs141110020	Chr.2: 99554396-99554396 on Build GRCh38
rs200443568	Chr.2: 99554420-99554420 on Build GRCh38
rs760098040	Chr.2: 99554457-99554457 on Build GRCh38
rs766875568	Chr.2: 99554401-99554401 on Build GRCh38
rs756690263	Chr.2: 99554455-99554455 on Build GRCh38
rs772657804	Chr.2: 99554486-99554486 on Build GRCh38
rs758389402	Chr.2: 99554448-99554448 on Build GRCh38
rs773374557	Chr.2: 99554407-99554407 on Build GRCh38
rs752486698	Chr.2: 99554446-99554446 on Build GRCh38
rs754085390	Chr.2: 99554435-99554435 on Build GRCh38
rs368703010	Chr.2: 99554449-99554449 on Build GRCh38
rs762394931	Chr.2: 99554399-99554399 on Build GRCh38

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