Product Details

SNP ID
rs72542769
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:143278813 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGCCTCTGAATTCTGAAGGGAGC[A/G]TGGCTTTCCTTCATGGCATGCCCAG
Phenotype
MIM: 138040
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NR3C1 PubMed Links

Gene Details

Gene
NR3C1
Gene Name
nuclear receptor subfamily 3 group C member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000176.2 5902 UTR 3 NP_000167.1
NM_001018074.1 5902 UTR 3 NP_001018084.1
NM_001018075.1 5902 UTR 3 NP_001018085.1
NM_001018076.1 5902 UTR 3 NP_001018086.1
NM_001018077.1 5902 UTR 3 NP_001018087.1
NM_001020825.1 5902 UTR 3 NP_001018661.1
NM_001024094.1 5902 UTR 3 NP_001019265.1
NM_001204258.1 5902 UTR 3 NP_001191187.1
NM_001204259.1 5902 UTR 3 NP_001191188.1
NM_001204260.1 5902 UTR 3 NP_001191189.1
NM_001204261.1 5902 UTR 3 NP_001191190.1
NM_001204262.1 5902 UTR 3 NP_001191191.1
NM_001204263.1 5902 UTR 3 NP_001191192.1
NM_001204264.1 5902 UTR 3 NP_001191193.1
NM_001204265.1 5902 Intron NP_001191194.1
XM_005268419.3 5902 Intron XP_005268476.1
XM_005268420.4 5902 Intron XP_005268477.1
XM_005268422.3 5902 Intron XP_005268479.1
XM_005268423.3 5902 Intron XP_005268480.1
XM_011537637.2 5902 UTR 3 XP_011535939.1
XM_017009397.1 5902 UTR 3 XP_016864886.1
XM_017009398.1 5902 UTR 3 XP_016864887.1

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