Product Details

SNP ID
rs115060981
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:17793438 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATCAAATTCTGTGTTTGATTGGTT[C/T]TATTTTATACTCAGCTTTATTTTAT
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 3625 UTR 3 NP_055947.1
XM_005249672.1 3625 UTR 3 XP_005249729.1
XM_005249673.4 3625 Intron XP_005249730.1
XM_011515229.1 3625 UTR 3 XP_011513531.1
XM_011515230.2 3625 UTR 3 XP_011513532.1
XM_011515231.2 3625 UTR 3 XP_011513533.1
XM_011515233.2 3625 UTR 3 XP_011513535.1
XM_017011893.1 3625 UTR 3 XP_016867382.1
XM_017011894.1 3625 UTR 3 XP_016867383.1
XM_017011895.1 3625 UTR 3 XP_016867384.1
XM_017011896.1 3625 UTR 3 XP_016867385.1
XM_017011897.1 3625 UTR 3 XP_016867386.1

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