Product Details

SNP ID
rs13194859
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:10895820 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TACTTCTAAAGACAACTGTGTTTGC[A/G]GACTGAACACAAAGTGTGCTCGGAA
Phenotype
MIM: 616799
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SYCP2L PubMed Links
Additional Information
For this assay, SNP(s) [rs116333610] 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
SYCP2L
Gene Name
synaptonemal complex protein 2 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040274.2 Intron NP_001035364.2

View Full Product Details