Product Details

SNP ID: rs590590
Assay Type: Functionally Tested
NCBI dbSNP Submissions: NA
Location: Chr.11:134072248 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGCACAAATGTAGTAAAAGAAAGG[A/G]AAATATGTGTGAATGAAGTTAGGAT
Phenotype: MIM: 606871
Polymorphism: A/G, Transition Substitution
Allele Nomenclature
Literature Links: JAM3 PubMed Links
Additional Information: For this assay, SNP(s) [rs116205587] are located under a probe 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

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001205329.1		Intron			NP_001192258.1
NM_032801.4		Intron			NP_116190.3