Product Details

SNP ID
rs202237610
Assay Type
Functionally tested
NCBI dbSNP Submissions
2
Location
Chr.1:36420608 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCTTTAGCAAGAGGGTTTGGAGCA[A/C]TGCTTTCCTGCAGAAACAGTTGCAT
Phenotype
MIM: 608854
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
OSCP1 PubMed Links

Gene Details

Gene
OSCP1
Gene Name
organic solute carrier partner 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_145047.4 943 Missense Mutation AGT,ATT S276I NP_659484.4
NM_206837.2 943 Intron NP_996668.1
XM_005270461.1 943 Missense Mutation AGT,ATT S286I XP_005270518.1
XM_005270462.1 943 Intron XP_005270519.1
XM_005270463.3 943 Intron XP_005270520.1
XM_011540680.2 943 Missense Mutation AGT,ATT S258I XP_011538982.1
XM_011540681.2 943 Missense Mutation AGT,ATT S248I XP_011538983.1
XM_017000303.1 943 Intron XP_016855792.1
XM_017000304.1 943 Intron XP_016855793.1

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