Product Details

SNP ID

rs201045149

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:58305103 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGTCCTGGGTTCCCTGTCCAGGCC[A/G]CCTGCCTCAGGCCCAGGGCCCTCCA

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	5357	Silent Mutation	GGC,GGT	G1825G	NP_001248764.1
NM_004758.3	5357	Silent Mutation	GGC,GGT	G1834G	NP_004749.2
NM_024418.2	5357	Silent Mutation	GGC,GGT	G1774G	NP_077729.1
XM_005257807.2	5357	Silent Mutation	GGC,GGT	G1825G	XP_005257864.1
XM_006722173.2	5357	Silent Mutation	GGC,GGT	G1834G	XP_006722236.1
XM_006722174.2	5357	Silent Mutation	GGC,GGT	G1827G	XP_006722237.1
XM_006722175.2	5357	Silent Mutation	GGC,GGT	G1774G	XP_006722238.1
XM_006722176.2	5357	Silent Mutation	GGC,GGT	G1557G	XP_006722239.1
XM_006722177.3	5357	Silent Mutation	GGC,GGT	G1394G	XP_006722240.1
XM_006722178.3	5357	Silent Mutation	GGC,GGT	G1394G	XP_006722241.1
XM_011525471.2	5357	Silent Mutation	GGC,GGT	G1355G	XP_011523773.1
XM_011525472.1	5357	Silent Mutation	GGC,GGT	G1338G	XP_011523774.1
XM_017025326.1	5357	Silent Mutation	GGC,GGT	G1834G	XP_016880815.1
XM_017025327.1	5357	Silent Mutation	GGC,GGT	G1795G	XP_016880816.1
XM_017025328.1	5357	Silent Mutation	GGC,GGT	G1731G	XP_016880817.1
XM_017025329.1	5357	Silent Mutation	GGC,GGT	G1554G	XP_016880818.1
XM_017025330.1	5357	Silent Mutation	GGC,GGT	G1554G	XP_016880819.1
XM_017025331.1	5357	Silent Mutation	GGC,GGT	G1545G	XP_016880820.1
XM_017025332.1	5357	Silent Mutation	GGC,GGT	G1494G	XP_016880821.1
XM_017025333.1	5357	Silent Mutation	GGC,GGT	G1268G	XP_016880822.1
XM_017025334.1	5357	Silent Mutation	GGC,GGT	G1217G	XP_016880823.1

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