Product Details

SNP ID
rs200217891
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:73485867 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCTTCTCTGTTGTATAGAATAA[C/T]GTTTTACAGGAAAAAATATGTGCTA
Phenotype
MIM: 104145
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
AFM PubMed Links

Gene Details

Gene
AFM
Gene Name
afamin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001133.2 312 Silent Mutation AAC,AAT N92N NP_001124.1
XM_017007842.1 312 Silent Mutation AAC,AAT N92N XP_016863331.1
XM_017007843.1 312 Silent Mutation AAC,AAT N92N XP_016863332.1
XM_017007844.1 312 Silent Mutation AAC,AAT N92N XP_016863333.1

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