Product Details

Primer Sequences

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Primer Chromosome Location

Chr.17: 67854376-67854617 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

BPTF

Entrez Gene ID

2186

Gene Name

bromodomain PHD finger transcription factor

Gene Aliases

FAC1, FALZ, NURF301

UniGene

Hs.444200

Gene Chromosome Location

Chr.17: 67825517-67984378 on Build GRCh38

Transcripts

NM_004459.6 NM_182641.3 XM_005257150.3 XM_005257151.3 XM_005257152.2 XM_005257153.3 XM_005257154.3 XM_005257155.3 XM_005257156.3 XM_005257157.3 XM_005257158.3 XM_005257159.2 XM_005257160.2 XM_005257161.3 XM_011524520.2 XM_011524521.2 XM_011524522.2 XM_011524523.2 XM_011524525.2 XM_011524526.2 XM_017024353.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
6848865	c.1196T>C	p.L399P	Chr.17: 67854522-67854522 on Build GRCh38
707551	c.1090C>T	p.L364L	Chr.17: 67854416-67854416 on Build GRCh38
1246197	c.1264_1266delGAG	p.E423delE	Chr.17: 67854590-67854592 on Build GRCh38
6612448	c.1206G>T	p.L402F	Chr.17: 67854532-67854532 on Build GRCh38
5853296	c.1133G>A	p.R378Q	Chr.17: 67854459-67854459 on Build GRCh38
7246396	c.1216G>C	p.E406Q	Chr.17: 67854542-67854542 on Build GRCh38
6147514	c.1276G>A	p.E426K	Chr.17: 67854602-67854602 on Build GRCh38
3378295	c.1184T>C	p.V395A	Chr.17: 67854510-67854510 on Build GRCh38
4665991	c.1233A>G	p.V411V	Chr.17: 67854559-67854559 on Build GRCh38
983286	c.1209T>C	p.L403L	Chr.17: 67854535-67854535 on Build GRCh38
304429	c.1281C>G	p.D427E	Chr.17: 67854607-67854607 on Build GRCh38
983284	c.1161A>C	p.I387I	Chr.17: 67854487-67854487 on Build GRCh38
983282	c.1095G>T	p.Q365H	Chr.17: 67854421-67854421 on Build GRCh38
983280	c.1061A>T	p.Y354F	Chr.17: 67854387-67854387 on Build GRCh38
5853295	c.1133G>A	p.R378Q	Chr.17: 67854459-67854459 on Build GRCh38
7246395	c.1216G>C	p.E406Q	Chr.17: 67854542-67854542 on Build GRCh38
6612434	c.1244A>C	p.E415A	Chr.17: 67854570-67854570 on Build GRCh38
707550	c.1090C>T	p.L364L	Chr.17: 67854416-67854416 on Build GRCh38
7158869	c.1231G>A	p.V411I	Chr.17: 67854557-67854557 on Build GRCh38
1680023	c.1105G>A	p.D369N	Chr.17: 67854431-67854431 on Build GRCh38
4665990	c.1233A>G	p.V411V	Chr.17: 67854559-67854559 on Build GRCh38
6848866	c.1196T>C	p.L399P	Chr.17: 67854522-67854522 on Build GRCh38
7158868	c.1231G>A	p.V411I	Chr.17: 67854557-67854557 on Build GRCh38
3378296	c.1184T>C	p.V395A	Chr.17: 67854510-67854510 on Build GRCh38
983279	c.1061A>T	p.Y354F	Chr.17: 67854387-67854387 on Build GRCh38
983281	c.1095G>T	p.Q365H	Chr.17: 67854421-67854421 on Build GRCh38
983283	c.1161A>C	p.I387I	Chr.17: 67854487-67854487 on Build GRCh38
983285	c.1209T>C	p.L403L	Chr.17: 67854535-67854535 on Build GRCh38
6612435	c.1244A>C	p.E415A	Chr.17: 67854570-67854570 on Build GRCh38
6612449	c.1206G>T	p.L402F	Chr.17: 67854532-67854532 on Build GRCh38
1680024	c.1105G>A	p.D369N	Chr.17: 67854431-67854431 on Build GRCh38
6147515	c.1276G>A	p.E426K	Chr.17: 67854602-67854602 on Build GRCh38
1246196	c.1264_1266delGAG	p.E423delE	Chr.17: 67854590-67854592 on Build GRCh38
304430	c.1281C>G	p.D427E	Chr.17: 67854607-67854607 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs146758771	Chr.17: 67854430-67854430 on Build GRCh38
rs771231934	Chr.17: 67854482-67854482 on Build GRCh38
rs774589699	Chr.17: 67854487-67854487 on Build GRCh38
rs761621400	Chr.17: 67854502-67854502 on Build GRCh38
rs991755344	Chr.17: 67854400-67854400 on Build GRCh38
rs914711386	Chr.17: 67854411-67854411 on Build GRCh38
rs759753871	Chr.17: 67854493-67854493 on Build GRCh38
rs369457219	Chr.17: 67854519-67854519 on Build GRCh38
rs145008089	Chr.17: 67854500-67854500 on Build GRCh38
rs765110277	Chr.17: 67854518-67854518 on Build GRCh38
rs777972120	Chr.17: 67854413-67854413 on Build GRCh38
rs141167344	Chr.17: 67854499-67854499 on Build GRCh38

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