Product Details

SNP ID
rs143205041
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:88535533 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAACAAGGTGGTGGCACTGTACTT[C/T]GCGGCGGCCCGGTGCGCGCCGAGCC
Phenotype
MIM: 615299
Polymorphism
C/T, Transition 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_001161625.1 433 Silent Mutation TTC,TTT F33F NP_001155097.1
NM_145283.2 433 Silent Mutation TTC,TTT F33F NP_660326.2
XM_005251727.3 433 Missense Mutation TTC,TTT F33F XP_005251784.1
XM_011518275.2 433 Missense Mutation TTC,TTT F33F XP_011516577.1
XM_011518276.2 433 Missense Mutation TTC,TTT F33F XP_011516578.1

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