Product Details

SNP ID
rs12913860
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:38459752 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCGGAGATGGGCTCCCTTGGGTAC[C/G]CTGGCTCCAGTCTCCTAGCAGCAGC
Phenotype
MIM: 616142
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM98B PubMed Links

Gene Details

Gene
FAM98B
Gene Name
family with sequence similarity 98 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_173611.3 Intron NP_775882.2

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