Product Details

SNP ID
rs56276483
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:100473966 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTAATGCGAAATTGGATTCTGAGC[A/C]TTTGTAGCAAAATCGCTGGGATCTG
Phenotype
MIM: 603826
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
NR1H4 PubMed Links

Gene Details

Gene
NR1H4
Gene Name
nuclear receptor subfamily 1 group H member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206977.1 194 UTR 5 NP_001193906.1
NM_001206978.1 194 UTR 5 NP_001193907.1
NM_001206979.1 194 UTR 5 NP_001193908.1
NM_001206992.1 194 Intron NP_001193921.1
NM_001206993.1 194 Intron NP_001193922.1
NM_005123.3 194 UTR 5 NP_005114.1
XM_006719719.2 194 Intron XP_006719782.1
XM_011539040.2 194 Intron XP_011537342.1
XM_011539041.2 194 Intron XP_011537343.1
XM_011539042.1 194 Intron XP_011537344.1

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