Product Details

SNP ID

rs17598603

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:84656980 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTACTGGGAAGGTCAGCTTCCTTT[C/G]TTTGGACTGTTCCTCCTTTGAGCTC

Phenotype

MIM: 162340 MIM: 616144

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

NMB PubMed Links

Additional Information

For this assay, SNP(s) [rs75197414] 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

NMB

Gene Name

neuromedin B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021077.3		Intron			NP_066563.2
NM_205858.1		Intron			NP_995580.1
XM_017022239.1		Intron			XP_016877728.1

Gene

WDR73

Gene Name

WD repeat domain 73

There are no transcripts associated with this gene.

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