Product Details

SNP ID
rs184459414
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:17794066 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTGTCACCTTTTCTGCAAAGAAGG[C/T]GCTTGAGTAGTTTGAAGTTTCTGTT
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 2997 Silent Mutation NP_055947.1
XM_005249672.1 2997 Silent Mutation XP_005249729.1
XM_005249673.4 2997 Intron XP_005249730.1
XM_011515229.1 2997 Silent Mutation XP_011513531.1
XM_011515230.2 2997 Silent Mutation XP_011513532.1
XM_011515231.2 2997 Silent Mutation XP_011513533.1
XM_011515233.2 2997 Silent Mutation XP_011513535.1
XM_017011893.1 2997 Silent Mutation XP_016867382.1
XM_017011894.1 2997 Silent Mutation XP_016867383.1
XM_017011895.1 2997 Silent Mutation XP_016867384.1
XM_017011896.1 2997 Silent Mutation XP_016867385.1
XM_017011897.1 2997 Silent Mutation XP_016867386.1

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