Product Details

SNP ID

rs67572077

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:4383717 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGGGTAGGAGTTACAATCGTACA[C/G]GCAGTGATGGGTCTGTGCCTGAGAT

Phenotype

MIM: 607645

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NSG1 PubMed Links

Additional Information

For this assay, SNP(s) [rs150467373] 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

NSG1

Gene Name

neuron specific gene family member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040101.1		Intron			NP_001035190.1
NM_001287763.1		Intron			NP_001274692.1
NM_001287764.1		Intron			NP_001274693.1
NM_014392.4		Intron			NP_055207.1
XM_017008022.1		Intron			XP_016863511.1

View Full Product Details