Product Details

SNP ID
rs200414575
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:72132334 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCATCCACGGGGTGCAGGACGG[G/T]GACCAAGGTGATGCGGGGGAAGGTC
Phenotype
MIM: 605207
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CYP26B1 PubMed Links

Gene Details

Gene
CYP26B1
Gene Name
cytochrome P450 family 26 subfamily B member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001277742.1 1235 Missense Mutation ACC,CCC T403P NP_001264671.1
NM_019885.3 1235 Missense Mutation ACC,CCC T478P NP_063938.1
XM_005264433.4 1235 Missense Mutation ACC,CCC T420P XP_005264490.1
XM_011532988.1 1235 Missense Mutation ACC,CCC T287P XP_011531290.1

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