Product Details

SNP ID
rs146062765
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:88535684 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCCCAGGAGATGCTGGACTTCATG[C/G]GCGAGCTGCATGGCGCCTGGCTGGC
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_001161625.1 584 Missense Mutation CGC,GGC R84G NP_001155097.1
NM_145283.2 584 Missense Mutation CGC,GGC R84G NP_660326.2
XM_005251727.3 584 Missense Mutation CGC,GGC R84G XP_005251784.1
XM_011518275.2 584 Missense Mutation CGC,GGC R84G XP_011516577.1
XM_011518276.2 584 Missense Mutation CGC,GGC R84G XP_011516578.1

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