Product Details

SNP ID
rs7875283
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:135664757 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GAGTGTGTGGCTGTGGTCGTGGTCT[G/T]CGAGAAGACAGAGAAGAATGGGGAA
Phenotype
MIM: 612903
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
LCN9 PubMed Links

Gene Details

Gene
LCN9
Gene Name
lipocalin 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001676.1 269 Missense Mutation TGC,TTC C90F NP_001001676.1
XM_017014712.1 269 Missense Mutation TGC,TTC C90F XP_016870201.1

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