Product Details

SNP ID
rs2154639
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:100578242 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTAAACACCACCTAGCCAGGCTTTT[G/T]GGGGAAAGAGTTCTTAGACTCTTCT
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 Intron NP_689841.3
XM_005250815.3 Intron XP_005250872.1
XM_011516899.1 Intron XP_011515201.1
XM_017013153.1 Intron XP_016868642.1
XM_017013154.1 Intron XP_016868643.1
XM_017013155.1 Intron XP_016868644.1
XM_017013156.1 Intron XP_016868645.1
XM_017013157.1 Intron XP_016868646.1
XM_017013158.1 Intron XP_016868647.1
XM_017013159.1 Intron XP_016868648.1
XM_017013160.1 Intron XP_016868649.1
XM_017013161.1 Intron XP_016868650.1
XM_017013162.1 Intron XP_016868651.1
XM_017013163.1 Intron XP_016868652.1
XM_017013164.1 Intron XP_016868653.1
XM_017013165.1 Intron XP_016868654.1

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