Product Details

SNP ID
rs13266724
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:81802901 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTTATTTTCCTGATGTTTCCCA[A/T]CCTTCAATGTTCAAAATTTATTTAG
Phenotype
MIM: 614903
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
SNX16 PubMed Links

Gene Details

Gene
SNX16
Gene Name
sorting nexin 16
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_022133.3 Intron NP_071416.2
NM_152836.2 Intron NP_690049.1
NM_152837.2 Intron NP_690050.1
XM_005251282.4 Intron XP_005251339.1
XM_005251283.2 Intron XP_005251340.1
XM_011517574.2 Intron XP_011515876.1

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