Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.9: 104772913-104773138 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: NIPSNAP3B
Entrez Gene ID: 55335
Gene Name: nipsnap homolog 3B
Gene Aliases: FP944, NIPSNAP3, SNAP1
UniGene: Hs.429294
Gene Chromosome Location: Chr.9: 104763741-104777764 on Build GRCh38
Transcripts: NM_018376.3 NR_130759.1 NR_130760.1 XM_011518839.1 XM_017014889.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
5625384	c.702G>A	p.Q234Q	Chr.9: 104773031-104773031 on Build GRCh38
5567761	c.695C>A	p.S232Y	Chr.9: 104773024-104773024 on Build GRCh38
3902732	c.726A>G	p.S242S	Chr.9: 104773055-104773055 on Build GRCh38
1103511	c.693T>A	p.V231V	Chr.9: 104773022-104773022 on Build GRCh38
1103510	c.670C>T	p.R224W	Chr.9: 104772999-104772999 on Build GRCh38
5024446	c.681C>G	p.V227V	Chr.9: 104773010-104773010 on Build GRCh38
5024266	c.725C>A	p.S242*	Chr.9: 104773054-104773054 on Build GRCh38
4806237	c.702G>C	p.Q234H	Chr.9: 104773031-104773031 on Build GRCh38
6726440	c.677G>T	p.S226I	Chr.9: 104773006-104773006 on Build GRCh38
106467	c.719C>T	p.P240L	Chr.9: 104773048-104773048 on Build GRCh38
1459097	c.671G>A	p.R224Q	Chr.9: 104773000-104773000 on Build GRCh38
752183	c.743A>T	p.*248L	Chr.9: 104773072-104773072 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs778348014	Chr.9: 104772984-104772984 on Build GRCh38
rs377506623	Chr.9: 104772962-104772962 on Build GRCh38
rs759656734	Chr.9: 104773015-104773015 on Build GRCh38
rs768505634	Chr.9: 104773060-104773060 on Build GRCh38
rs764481365	Chr.9: 104773023-104773023 on Build GRCh38
rs529659668	Chr.9: 104773003-104773003 on Build GRCh38
rs779445447	Chr.9: 104773052-104773052 on Build GRCh38
rs769748783	Chr.9: 104773072-104773072 on Build GRCh38
rs552388877	Chr.9: 104773089-104773089 on Build GRCh38
rs957808488	Chr.9: 104772995-104772995 on Build GRCh38
rs754178768	Chr.9: 104773027-104773027 on Build GRCh38
rs772219262	Chr.9: 104773100-104773100 on Build GRCh38
rs775435890	Chr.9: 104773111-104773111 on Build GRCh38
rs767772776	Chr.9: 104773018-104773018 on Build GRCh38
rs779967255	Chr.9: 104773000-104773000 on Build GRCh38
rs780989418	Chr.9: 104773063-104773063 on Build GRCh38
rs753232095	Chr.9: 104773020-104773020 on Build GRCh38
rs750147301	Chr.9: 104773038-104773038 on Build GRCh38
rs150554330	Chr.9: 104772999-104772999 on Build GRCh38
rs750851064	Chr.9: 104773029-104773029 on Build GRCh38
rs756325897	Chr.9: 104772982-104772982 on Build GRCh38
rs562267988	Chr.9: 104772956-104772956 on Build GRCh38
rs149753675	Chr.9: 104773022-104773022 on Build GRCh38
rs778056091	Chr.9: 104772964-104772964 on Build GRCh38
rs771297073	Chr.9: 104773007-104773007 on Build GRCh38
rs745360995	Chr.9: 104772996-104772996 on Build GRCh38
rs750456883	Chr.9: 104772978-104772978 on Build GRCh38
rs774759408	Chr.9: 104773009-104773009 on Build GRCh38
rs753471162	Chr.9: 104772976-104772976 on Build GRCh38
rs780408589	Chr.9: 104772986-104772986 on Build GRCh38
rs756892647	Chr.9: 104772979-104772979 on Build GRCh38
rs368271075	Chr.9: 104773078-104773078 on Build GRCh38
rs746900711	Chr.9: 104773059-104773059 on Build GRCh38
rs778507463	Chr.9: 104773034-104773034 on Build GRCh38
rs747869885	Chr.9: 104773064-104773064 on Build GRCh38
rs763192312	Chr.9: 104773006-104773006 on Build GRCh38
rs140617020	Chr.9: 104773048-104773048 on Build GRCh38
rs56270385	Chr.9: 104773004-104773004 on Build GRCh38

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