Product Details

SNP ID
rs17852066
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:88535661 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTCTTCGTGTCAGCCGACGGCAGCT[C/G]CCAGGAGATGCTGGACTTCATGCGC
Phenotype
MIM: 615299
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
NXNL2 PubMed Links

Gene Details

Gene
NXNL2
Gene Name
nucleoredoxin-like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001161625.1 561 Missense Mutation TCC,TGC S76C NP_001155097.1
NM_145283.2 561 Missense Mutation TCC,TGC S76C NP_660326.2
XM_005251727.3 561 Missense Mutation TCC,TGC S76C XP_005251784.1
XM_011518275.2 561 Missense Mutation TCC,TGC S76C XP_011516577.1
XM_011518276.2 561 Missense Mutation TCC,TGC S76C XP_011516578.1

View Full Product Details