Product Details

SNP ID
rs111701816
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:46550346 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACTCCTCCAGAAGGCCCTGGTC[A/C]TTGTGAGGCCCAACAGATGTCATAT
Phenotype
MIM: 605994
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CYP39A1 PubMed Links

Gene Details

Gene
CYP39A1
Gene Name
cytochrome P450 family 39 subfamily A member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278738.1 1468 UTR 3 NP_001265667.1
NM_001278739.1 1468 UTR 3 NP_001265668.1
NM_016593.4 1468 UTR 3 NP_057677.2
XM_005249171.3 1468 Intron XP_005249228.1
XM_011514658.1 1468 UTR 3 XP_011512960.1
XM_017010921.1 1468 Intron XP_016866410.1
XM_017010922.1 1468 Intron XP_016866411.1
XM_017010923.1 1468 Intron XP_016866412.1
XM_017010924.1 1468 UTR 3 XP_016866413.1
XM_017010925.1 1468 UTR 3 XP_016866414.1

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