Product Details

SNP ID
rs201004595
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:100573959 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGATAGAAAACTAGAATAGTCTTTC[G/T]GCTGTGAAGTAAACAGAGAGGTCAG
Phenotype
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SNX31 PubMed Links

Gene Details

Gene
SNX31
Gene Name
sorting nexin 31
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152628.3 1460 Missense Mutation NP_689841.3
XM_005250815.3 1460 Missense Mutation XP_005250872.1
XM_011516899.1 1460 Missense Mutation XP_011515201.1
XM_017013153.1 1460 Intron XP_016868642.1
XM_017013154.1 1460 Missense Mutation XP_016868643.1
XM_017013155.1 1460 Intron XP_016868644.1
XM_017013156.1 1460 Missense Mutation XP_016868645.1
XM_017013157.1 1460 Missense Mutation XP_016868646.1
XM_017013158.1 1460 Missense Mutation XP_016868647.1
XM_017013159.1 1460 Missense Mutation XP_016868648.1
XM_017013160.1 1460 Missense Mutation XP_016868649.1
XM_017013161.1 1460 Missense Mutation XP_016868650.1
XM_017013162.1 1460 Missense Mutation XP_016868651.1
XM_017013163.1 1460 Missense Mutation XP_016868652.1
XM_017013164.1 1460 Intron XP_016868653.1
XM_017013165.1 1460 Intron XP_016868654.1

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