Product Details

SNP ID
rs17851612
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:36418180 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGGCGAGCAAATCGTCCCCTTTGC[C/T]GGTGCTCAGCCTTGGCTGCTCCGTG
Phenotype
MIM: 608854
Polymorphism
C/T, Transition 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 1215 Missense Mutation AGC,GGC S367G NP_659484.4
NM_206837.2 1215 Intron NP_996668.1
XM_005270461.1 1215 Missense Mutation AGC,GGC S377G XP_005270518.1
XM_005270462.1 1215 UTR 3 XP_005270519.1
XM_005270463.3 1215 Intron XP_005270520.1
XM_011540680.2 1215 Missense Mutation AGC,GGC S349G XP_011538982.1
XM_011540681.2 1215 Missense Mutation AGC,GGC S339G XP_011538983.1
XM_017000303.1 1215 UTR 3 XP_016855792.1
XM_017000304.1 1215 Intron XP_016855793.1

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