Product Details

SNP ID
rs117121536
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:17794713 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAATGTAAAAAGTGATCTGTAAACT[C/T]TGTAATATTATACAAATATTCTTAG
Phenotype
MIM: 606589
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SNX13 PubMed Links

Gene Details

Gene
SNX13
Gene Name
sorting nexin 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015132.4 Intron NP_055947.1
XM_005249672.1 Intron XP_005249729.1
XM_005249673.4 Intron XP_005249730.1
XM_011515229.1 Intron XP_011513531.1
XM_011515230.2 Intron XP_011513532.1
XM_011515231.2 Intron XP_011513533.1
XM_011515233.2 Intron XP_011513535.1
XM_017011893.1 Intron XP_016867382.1
XM_017011894.1 Intron XP_016867383.1
XM_017011895.1 Intron XP_016867384.1
XM_017011896.1 Intron XP_016867385.1
XM_017011897.1 Intron XP_016867386.1

View Full Product Details