Product Details

SNP ID
rs141491349
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:58302161 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCCTCTGAATGCCACAGTGTTAAC[A/G]CAGAAGAACGGGGGCTCTGGGCCCA
Phenotype
MIM: 610764
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
TSPOAP1 PubMed Links

Gene Details

Gene
TSPOAP1
Gene Name
TSPO associated protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261835.1 4895 UTR 3 NP_001248764.1
NM_004758.3 4895 UTR 3 NP_004749.2
NM_024418.2 4895 UTR 3 NP_077729.1
XM_005257807.2 4895 UTR 3 XP_005257864.1
XM_006722173.2 4895 UTR 3 XP_006722236.1
XM_006722174.2 4895 UTR 3 XP_006722237.1
XM_006722175.2 4895 UTR 3 XP_006722238.1
XM_006722176.2 4895 UTR 3 XP_006722239.1
XM_006722177.3 4895 UTR 3 XP_006722240.1
XM_006722178.3 4895 UTR 3 XP_006722241.1
XM_011525471.2 4895 UTR 3 XP_011523773.1
XM_011525472.1 4895 UTR 3 XP_011523774.1
XM_017025326.1 4895 Intron XP_016880815.1
XM_017025327.1 4895 UTR 3 XP_016880816.1
XM_017025328.1 4895 UTR 3 XP_016880817.1
XM_017025329.1 4895 UTR 3 XP_016880818.1
XM_017025330.1 4895 Intron XP_016880819.1
XM_017025331.1 4895 Intron XP_016880820.1
XM_017025332.1 4895 Intron XP_016880821.1
XM_017025333.1 4895 Intron XP_016880822.1
XM_017025334.1 4895 Intron XP_016880823.1

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