Product Details

SNP ID

rs10415665

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:13013088 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTAAAAAAAAAACCTTTAAAAACCC[A/C]AAACCTCCCCTCCAAGTCCCTTTCG

Phenotype

MIM: 164005

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

NFIX PubMed Links

Additional Information

For this assay, SNP(s) [rs77637881] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

NFIX

Gene Name

nuclear factor I X

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001271043.2		Intron			NP_001257972.1
NM_001271044.2		Intron			NP_001257973.1
NM_002501.3		Intron			NP_002492.2
XM_005259917.4		Intron			XP_005259974.1
XM_005259918.4		Intron			XP_005259975.1
XM_005259919.3		Intron			XP_005259976.1
XM_005259920.3		Intron			XP_005259977.1
XM_006722760.2		Intron			XP_006722823.1
XM_011528040.1		Intron			XP_011526342.1
XM_017026837.1		Intron			XP_016882326.1

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