Product Details

SNP ID
rs62449272
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:84124705 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCAATACACCCATGTTACAACAAG[C/T]ACATGTACCCCCTGGATCTAAAATA
Phenotype
MIM: 610201 MIM: 615410
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
CEP162 PubMed Links

Gene Details

Gene
CEP162
Gene Name
centrosomal protein 162
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286206.1 4815 UTR 3 NP_001273135.1
NM_014895.3 4815 UTR 3 NP_055710.2
XM_005248674.3 4815 UTR 3 XP_005248731.1
XM_005248678.3 4815 Intron XP_005248735.1
XM_006715380.2 4815 UTR 3 XP_006715443.1
XM_011535592.2 4815 UTR 3 XP_011533894.1
XM_011535594.2 4815 Intron XP_011533896.1
XM_017010483.1 4815 UTR 3 XP_016865972.1
XM_017010484.1 4815 UTR 3 XP_016865973.1
Gene
MRAP2
Gene Name
melanocortin 2 receptor accessory protein 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138409.2 4815 Intron NP_612418.2
XM_011535400.2 4815 Intron XP_011533702.1
XM_017010219.1 4815 Intron XP_016865708.1
XM_017010220.1 4815 Intron XP_016865709.1
XM_017010221.1 4815 Intron XP_016865710.1

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