Product Details

SNP ID
rs3894261
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:80183824 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCCCCTTCTCTTGTACCCCCACCC[C/T]CGCCCGCTGCCGAGGCTCCAGATGG
Phenotype
MIM: 616639
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRDM8 PubMed Links
Additional Information
For this assay, SNP(s) [rs141241985] 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
PRDM8
Gene Name
PR domain 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099403.1 407 Intron NP_001092873.1
NM_020226.3 407 Intron NP_064611.3
XM_005263144.2 407 Intron XP_005263201.1
XM_005263145.2 407 Intron XP_005263202.1
XM_005263146.4 407 Intron XP_005263203.1
XM_011532133.2 407 UTR 5 XP_011530435.1
XM_011532135.2 407 UTR 5 XP_011530437.1
XM_011532140.2 407 Intron XP_011530442.1
XM_011532141.2 407 Intron XP_011530443.1
XM_017008468.1 407 Intron XP_016863957.1
XM_017008469.1 407 Intron XP_016863958.1
XM_017008470.1 407 Intron XP_016863959.1

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