Product Details

SNP ID
rs12526640
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:121079835 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAGGAAAATGCATAACAAATAAGAG[G/T]AGAATGCTTATCAGTATGAAATAAC
Phenotype
MIM: 615867
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
TBC1D32 PubMed Links

Gene Details

Gene
TBC1D32
Gene Name
TBC1 domain family member 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_152730.5 4962 UTR 3 NP_689943.4
XM_005266861.2 4962 UTR 3 XP_005266918.1
XM_011535569.1 4962 UTR 3 XP_011533871.1
XM_011535570.1 4962 UTR 3 XP_011533872.1
XM_011535571.2 4962 UTR 3 XP_011533873.1
XM_011535574.1 4962 UTR 3 XP_011533876.1
XM_011535575.2 4962 Intron XP_011533877.1
XM_011535576.2 4962 Intron XP_011533878.1
XM_011535580.2 4962 UTR 3 XP_011533882.1
XM_011535582.2 4962 Intron XP_011533884.1
XM_011535585.2 4962 Intron XP_011533887.1
XM_017010397.1 4962 UTR 3 XP_016865886.1
XM_017010398.1 4962 UTR 3 XP_016865887.1
XM_017010399.1 4962 UTR 3 XP_016865888.1
XM_017010400.1 4962 UTR 3 XP_016865889.1
XM_017010401.1 4962 UTR 3 XP_016865890.1
XM_017010402.1 4962 Intron XP_016865891.1
XM_017010403.1 4962 Intron XP_016865892.1
XM_017010404.1 4962 UTR 3 XP_016865893.1
XM_017010405.1 4962 Intron XP_016865894.1

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