Product Details

SNP ID
rs12943408
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:82051520 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCACCTGCTGGCGGGCCCGGGAGA[A/T]CCAGGTGCGCAGCAGCAGCCGCAGG
Phenotype
MIM: 601934 MIM: 602578
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
DUS1L PubMed Links
Additional Information
For this assay, SNP(s) [rs189385594] 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
DUS1L
Gene Name
dihydrouridine synthase 1 like
There are no transcripts associated with this gene.

Gene
GPS1
Gene Name
G protein pathway suppressor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321089.1 255 Intron NP_001308018.1
NM_001321090.1 255 Intron NP_001308019.1
NM_001321091.1 255 Intron NP_001308020.1
NM_001321092.1 255 Intron NP_001308021.1
NM_001321093.1 255 Intron NP_001308022.1
NM_004127.5 255 Intron NP_004118.3
NM_212492.2 255 Intron NP_997657.1
XM_005256350.1 255 Intron XP_005256407.1
XM_005256353.1 255 Intron XP_005256410.1
XM_005256359.1 255 Intron XP_005256416.1
XM_005256360.3 255 Intron XP_005256417.1
XM_011523569.1 255 Intron XP_011521871.1
XM_011523570.1 255 Intron XP_011521872.1
XM_017024524.1 255 Intron XP_016880013.1
XM_017024525.1 255 Intron XP_016880014.1
XM_017024526.1 255 Intron XP_016880015.1
XM_017024527.1 255 Intron XP_016880016.1
XM_017024528.1 255 UTR 5 XP_016880017.1
XM_017024529.1 255 UTR 5 XP_016880018.1
XM_017024530.1 255 UTR 5 XP_016880019.1
XM_017024531.1 255 Intron XP_016880020.1
XM_017024532.1 255 Intron XP_016880021.1
XM_017024533.1 255 Intron XP_016880022.1
XM_017024534.1 255 Intron XP_016880023.1
XM_017024535.1 255 Intron XP_016880024.1
Gene
RFNG
Gene Name
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002917.1 255 Missense Mutation ATC,TTC I83F NP_002908.1
XM_011523587.2 255 Intron XP_011521889.1

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