Product Details

SNP ID
rs28596775
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:39518826 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGTGGGGGTCCTGGGGGAGAGGGGG[G/T]TGGTCAGGGATCTGAGATCCCCAAG
Phenotype
MIM: 607919
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SELV PubMed Links

Gene Details

Gene
SELV
Gene Name
selenoprotein V
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_182704.1 Intron NP_874363.1

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