Product Details

SNP ID
rs16876339
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:85513753 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAATTACTATACATTGTGACCTCAA[C/T]GGACTGCTAATCTATATGAAATTAA
Phenotype
MIM: 616105
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SNX14 PubMed Links

Gene Details

Gene
SNX14
Gene Name
sorting nexin 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297614.2 Intron NP_001284543.1
NM_001304479.1 Intron NP_001291408.1
NM_020468.5 Intron NP_065201.1
NM_153816.5 Intron NP_722523.1
XM_005248738.3 Intron XP_005248795.1
XM_005248740.3 Intron XP_005248797.1
XM_011535977.2 Intron XP_011534279.1
XM_011535979.1 Intron XP_011534281.1
XM_017011090.1 Intron XP_016866579.1
XM_017011091.1 Intron XP_016866580.1
XM_017011092.1 Intron XP_016866581.1
XM_017011093.1 Intron XP_016866582.1
XM_017011094.1 Intron XP_016866583.1
XM_017011095.1 Intron XP_016866584.1
XM_017011096.1 Intron XP_016866585.1
XM_017011097.1 Intron XP_016866586.1
XM_017011098.1 Intron XP_016866587.1
XM_017011099.1 Intron XP_016866588.1
XM_017011100.1 Intron XP_016866589.1
XM_017011101.1 Intron XP_016866590.1

View Full Product Details