Product Details

Primer Sequences

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Primer Chromosome Location

Chr.1: 190099016-190099241 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

BRINP3

Entrez Gene ID

339479

Gene Name

BMP/retinoic acid inducible neural specific 3

Gene Aliases

DBCCR1L, DBCCR1L1, FAM5C

UniGene

Hs.65765

Gene Chromosome Location

Chr.1: 190097662-190477997 on Build GRCh38

Transcripts

NM_001317188.1 NM_199051.2 XM_011509472.2 XM_011509475.2 XM_011509476.2 XM_017001125.1 XM_017001126.1 XM_017001127.1 XM_017001128.1 XM_017001129.1 XM_017001130.1 XM_017001131.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
901276	c.1274C>T	p.S425L	Chr.1: 190099045-190099045 on Build GRCh38
6478743	c.1245C>T	p.L415L	Chr.1: 190099074-190099074 on Build GRCh38
6659899	c.1254C>G	p.S418R	Chr.1: 190099065-190099065 on Build GRCh38
7198527	c.1297G>A	p.V433M	Chr.1: 190099022-190099022 on Build GRCh38
4764200	c.1229G>A	p.C410Y	Chr.1: 190099090-190099090 on Build GRCh38
1337274	c.1302C>T	p.V434V	Chr.1: 190099017-190099017 on Build GRCh38
4524990	c.1300G>A	p.V434I	Chr.1: 190099019-190099019 on Build GRCh38
368443	c.1254C>T	p.S418S	Chr.1: 190099065-190099065 on Build GRCh38
677458	c.1280C>A	p.T427K	Chr.1: 190099039-190099039 on Build GRCh38
5705110	c.1266G>T	p.E422D	Chr.1: 190099053-190099053 on Build GRCh38
3863896	c.1285C>T	p.P429S	Chr.1: 190099034-190099034 on Build GRCh38
3863897	c.1236G>A	p.E412E	Chr.1: 190099083-190099083 on Build GRCh38
107420	c.1234G>A	p.E412K	Chr.1: 190099085-190099085 on Build GRCh38
6508404	c.1261G>T	p.E421*	Chr.1: 190099058-190099058 on Build GRCh38
399853	c.1253G>A	p.S418N	Chr.1: 190099066-190099066 on Build GRCh38
3667041	c.1185-2A>G	p.?	Chr.1: 190099136-190099136 on Build GRCh38
386200	c.1264G>A	p.E422K	Chr.1: 190099055-190099055 on Build GRCh38
6508403	c.1300G>T	p.V434F	Chr.1: 190099019-190099019 on Build GRCh38
5914629	c.1217C>T	p.S406F	Chr.1: 190099102-190099102 on Build GRCh38
1317596	c.1207C>T	p.R403C	Chr.1: 190099112-190099112 on Build GRCh38
7077732	c.1229G>T	p.C410F	Chr.1: 190099090-190099090 on Build GRCh38
5414617	c.1259C>T	p.S420L	Chr.1: 190099060-190099060 on Build GRCh38
6492869	c.1269G>C	p.T423T	Chr.1: 190099050-190099050 on Build GRCh38
4436355	c.1208G>A	p.R403H	Chr.1: 190099111-190099111 on Build GRCh38
463621	c.1275G>A	p.S425S	Chr.1: 190099044-190099044 on Build GRCh38
463622	c.1268C>T	p.T423M	Chr.1: 190099051-190099051 on Build GRCh38
3976738	c.1249G>T	p.G417C	Chr.1: 190099070-190099070 on Build GRCh38
3789254	c.1281G>A	p.T427T	Chr.1: 190099038-190099038 on Build GRCh38
4433265	c.1188C>A	p.T396T	Chr.1: 190099131-190099131 on Build GRCh38
6060309	c.1270C>A	p.H424N	Chr.1: 190099049-190099049 on Build GRCh38
397083	c.1224C>G	p.L408L	Chr.1: 190099095-190099095 on Build GRCh38
3480461	c.1291G>A	p.D431N	Chr.1: 190099028-190099028 on Build GRCh38
2123635	c.1234G>C	p.E412Q	Chr.1: 190099085-190099085 on Build GRCh38
3740882	c.1269G>A	p.T423T	Chr.1: 190099050-190099050 on Build GRCh38
3480462	c.1286C>T	p.P429L	Chr.1: 190099033-190099033 on Build GRCh38
2123637	c.1192A>G	p.T398A	Chr.1: 190099127-190099127 on Build GRCh38
7302140	c.1185A>C	p.R395S	Chr.1: 190099134-190099134 on Build GRCh38
2123632	c.1287G>A	p.P429P	Chr.1: 190099032-190099032 on Build GRCh38
4026231	c.1239C>T	p.N413N	Chr.1: 190099080-190099080 on Build GRCh38
2123633	c.1261G>A	p.E421K	Chr.1: 190099058-190099058 on Build GRCh38
373942	c.1281G>T	p.T427T	Chr.1: 190099038-190099038 on Build GRCh38
901277	c.1224C>A	p.L408L	Chr.1: 190099095-190099095 on Build GRCh38
4808689	c.1249G>A	p.G417S	Chr.1: 190099070-190099070 on Build GRCh38
388893	c.1194C>A	p.T398T	Chr.1: 190099125-190099125 on Build GRCh38
371639	c.1274C>A	p.S425*	Chr.1: 190099045-190099045 on Build GRCh38
424859	c.1296G>A	p.Q432Q	Chr.1: 190099023-190099023 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs376124518	Chr.1: 190099139-190099139 on Build GRCh38
rs552714085	Chr.1: 190099210-190099210 on Build GRCh38
rs748884368	Chr.1: 190099077-190099077 on Build GRCh38
rs34098782	Chr.1: 190099078-190099078 on Build GRCh38
rs757210693	Chr.1: 190099038-190099038 on Build GRCh38
rs370578801	Chr.1: 190099145-190099145 on Build GRCh38
rs1016373683	Chr.1: 190099199-190099199 on Build GRCh38
rs963448813	Chr.1: 190099211-190099211 on Build GRCh38
rs764002569	Chr.1: 190099135-190099135 on Build GRCh38
rs749022277	Chr.1: 190099175-190099175 on Build GRCh38
rs932101955	Chr.1: 190099125-190099125 on Build GRCh38
rs539008222	Chr.1: 190099198-190099198 on Build GRCh38
rs779404004	Chr.1: 190099173-190099173 on Build GRCh38
rs781215603	Chr.1: 190099155-190099155 on Build GRCh38
rs755712395	Chr.1: 190099162-190099162 on Build GRCh38
rs760751290	Chr.1: 190099113-190099113 on Build GRCh38
rs911953658	Chr.1: 190099160-190099160 on Build GRCh38
rs373147254	Chr.1: 190099137-190099137 on Build GRCh38
rs762332585	Chr.1: 190099104-190099104 on Build GRCh38
rs759653868	Chr.1: 190099134-190099134 on Build GRCh38
rs769108806	Chr.1: 190099079-190099079 on Build GRCh38
rs138103319	Chr.1: 190099161-190099161 on Build GRCh38
rs769342168	Chr.1: 190099071-190099071 on Build GRCh38
rs774680022	Chr.1: 190099093-190099093 on Build GRCh38
rs768148345	Chr.1: 190099184-190099184 on Build GRCh38
rs745308648	Chr.1: 190099051-190099051 on Build GRCh38
rs567209093	Chr.1: 190099187-190099187 on Build GRCh38
rs546624036	Chr.1: 190099114-190099114 on Build GRCh38
rs754129370	Chr.1: 190099130-190099130 on Build GRCh38
rs772531253	Chr.1: 190099112-190099112 on Build GRCh38
rs775267735	Chr.1: 190099075-190099075 on Build GRCh38
rs148343462	Chr.1: 190099085-190099085 on Build GRCh38
rs866895040	Chr.1: 190099055-190099055 on Build GRCh38
rs1036264238	Chr.1: 190099159-190099159 on Build GRCh38
rs780878224	Chr.1: 190099044-190099044 on Build GRCh38
rs555067902	Chr.1: 190099183-190099183 on Build GRCh38

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