Product Details

SNP ID
rs7980659
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:95030551 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ATAAGACATGAACCAGGGGTAGGAG[G/T]CCATAAGTAAGATGGGAATGTGATG
Phenotype
MIM: 601529
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
NR2C1 PubMed Links

Gene Details

Gene
NR2C1
Gene Name
nuclear receptor subfamily 2 group C member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001032287.2 1972 UTR 3 NP_001027458.1
NM_001127362.1 1972 UTR 3 NP_001120834.1
NM_003297.3 1972 Intron NP_003288.2
XM_005269133.2 1972 Intron XP_005269190.1
XM_006719584.2 1972 Intron XP_006719647.1
XM_006719585.2 1972 Intron XP_006719648.1
XM_011538716.2 1972 Intron XP_011537018.1
XM_011538717.2 1972 Intron XP_011537019.1

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