Product Details

SNP ID
rs138558556
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:72132275 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCCGTCTCCGGCAGGATCTCGTT[C/G]TGGTTGGAGTCCAGGCCAAAGAACT
Phenotype
MIM: 605207
Polymorphism
C/G, 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 1294 Missense Mutation CAC,CAG H422Q NP_001264671.1
NM_019885.3 1294 Missense Mutation CAC,CAG H497Q NP_063938.1
XM_005264433.4 1294 Missense Mutation CAC,CAG H439Q XP_005264490.1
XM_011532988.1 1294 Missense Mutation CAC,CAG H306Q XP_011531290.1

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