Product Details

SNP ID
rs296364
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:47872441 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTCCGTCACTCTACTCACACGGGG[A/G]CTTCTGATTCTGCCTCAAACGTGGC
Phenotype
MIM: 125263
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LINC01595 PubMed Links
Additional Information
For this assay, SNP(s) [rs62529871] 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

Gene
LINC01595
Gene Name
long intergenic non-protein coding RNA 1595
There are no transcripts associated with this gene.

Gene
SULT2A1
Gene Name
sulfotransferase family 2A member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003167.3 Intron NP_003158.2

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