Product Details

SNP ID

rs201985313

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:58305065 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGAGCCCAGCTCCTCACTGACCTGA[C/T]TCTCAGCCTGGGGTGTCCTGGGTTC

Phenotype

MIM: 610764

Polymorphism

C/T, 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	5395	Missense Mutation	AAT,AGT	N1838S	NP_001248764.1
NM_004758.3	5395	Missense Mutation	AAT,AGT	N1847S	NP_004749.2
NM_024418.2	5395	Missense Mutation	AAT,AGT	N1787S	NP_077729.1
XM_005257807.2	5395	Missense Mutation	AAT,AGT	N1838S	XP_005257864.1
XM_006722173.2	5395	Missense Mutation	AAT,AGT	N1847S	XP_006722236.1
XM_006722174.2	5395	Missense Mutation	AAT,AGT	N1840S	XP_006722237.1
XM_006722175.2	5395	Missense Mutation	AAT,AGT	N1787S	XP_006722238.1
XM_006722176.2	5395	Missense Mutation	AAT,AGT	N1570S	XP_006722239.1
XM_006722177.3	5395	Missense Mutation	AAT,AGT	N1407S	XP_006722240.1
XM_006722178.3	5395	Missense Mutation	AAT,AGT	N1407S	XP_006722241.1
XM_011525471.2	5395	Missense Mutation	AAT,AGT	N1368S	XP_011523773.1
XM_011525472.1	5395	Missense Mutation	AAT,AGT	N1351S	XP_011523774.1
XM_017025326.1	5395	Missense Mutation	AAT,AGT	N1847S	XP_016880815.1
XM_017025327.1	5395	Missense Mutation	AAT,AGT	N1808S	XP_016880816.1
XM_017025328.1	5395	Missense Mutation	AAT,AGT	N1744S	XP_016880817.1
XM_017025329.1	5395	Missense Mutation	AAT,AGT	N1567S	XP_016880818.1
XM_017025330.1	5395	Missense Mutation	AAT,AGT	N1567S	XP_016880819.1
XM_017025331.1	5395	Missense Mutation	AAT,AGT	N1558S	XP_016880820.1
XM_017025332.1	5395	Missense Mutation	AAT,AGT	N1507S	XP_016880821.1
XM_017025333.1	5395	Missense Mutation	AAT,AGT	N1281S	XP_016880822.1
XM_017025334.1	5395	Missense Mutation	AAT,AGT	N1230S	XP_016880823.1

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