Product Details

SNP ID
rs442234
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:11978304 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGAGCTGGCTTCCCCCAGGAGCTGA[A/G]GTAGGTTGGTGTAAGTGCAGGCCCT
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SNX29 PubMed Links

Gene Details

Gene
SNX29
Gene Name
sorting nexin 29
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032167.4 Intron NP_115543.3
XM_005255682.3 Intron XP_005255739.1
XM_005255683.3 Intron XP_005255740.1
XM_011522738.2 Intron XP_011521040.1
XM_011522741.2 Intron XP_011521043.1
XM_011522743.2 Intron XP_011521045.1
XM_011522744.2 Intron XP_011521046.1
XM_017023871.1 Intron XP_016879360.1
XM_017023872.1 Intron XP_016879361.1
XM_017023873.1 Intron XP_016879362.1
XM_017023874.1 Intron XP_016879363.1
XM_017023875.1 Intron XP_016879364.1
XM_017023876.1 Intron XP_016879365.1
XM_017023877.1 Intron XP_016879366.1
XM_017023878.1 Intron XP_016879367.1

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