Product Details

SNP ID
rs35486539
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35436120 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCATACTTTACCTATCAGACTTG[C/T]TATCAAGATTATGCCAGCCTCATGA
Phenotype
MIM: 614955 MIM: 614957
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SLFN12 PubMed Links
Additional Information
For this assay, SNP(s) [rs80207209] 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
SLFN12
Gene Name
schlafen family member 12
There are no transcripts associated with this gene.

Gene
SLFN13
Gene Name
schlafen family member 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_144682.5 7445 UTR 3 NP_653283.3
XM_005257922.2 7445 Intron XP_005257979.1
XM_011524383.2 7445 Intron XP_011522685.1
XM_017024232.1 7445 Intron XP_016879721.1
XM_017024233.1 7445 Intron XP_016879722.1

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