Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 138040 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR3C1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Global
|
Caucasian
|
CEPH (CEU)
|
|||||||||
EAS
|
African American
|
YRI (Yoruba)
|
|||||||||
SAS
|
Japanese
|
JPT (Japanese)
|
|||||||||
AFR
|
Chinese
|
CHB (Han Chinese)
|
|||||||||
EUR
|
|||||||||||
AMR
|
NR3C1 - nuclear receptor subfamily 3 group C member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000176.2 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | NP_000167.1 | |
NM_001018074.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | NP_001018084.1 | |
NM_001018075.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | NP_001018085.1 | |
NM_001018076.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | NP_001018086.1 | |
NM_001018077.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | NP_001018087.1 | |
NM_001020825.1 | 2790 | Intron | NP_001018661.1 | |||
NM_001024094.1 | 2790 | Silent Mutation | AAC,AAT | N,N 767 | NP_001019265.1 | |
NM_001204258.1 | 2790 | Silent Mutation | AAC,AAT | N,N 740 | NP_001191187.1 | |
NM_001204259.1 | 2790 | Silent Mutation | AAC,AAT | N,N 681 | NP_001191188.1 | |
NM_001204260.1 | 2790 | Silent Mutation | AAC,AAT | N,N 677 | NP_001191189.1 | |
NM_001204261.1 | 2790 | Silent Mutation | AAC,AAT | N,N 669 | NP_001191190.1 | |
NM_001204262.1 | 2790 | Silent Mutation | AAC,AAT | N,N 451 | NP_001191191.1 | |
NM_001204263.1 | 2790 | Silent Mutation | AAC,AAT | N,N 436 | NP_001191192.1 | |
NM_001204264.1 | 2790 | Silent Mutation | AAC,AAT | N,N 431 | NP_001191193.1 | |
NM_001204265.1 | 2790 | Intron | NP_001191194.1 | |||
XM_005268419.3 | 2790 | Silent Mutation | AAC,AAT | N,N 767 | XP_005268476.1 | |
XM_005268420.4 | 2790 | Silent Mutation | AAC,AAT | N,N 767 | XP_005268477.1 | |
XM_005268422.3 | 2790 | Silent Mutation | AAC,AAT | N,N 767 | XP_005268479.1 | |
XM_005268423.3 | 2790 | Silent Mutation | AAC,AAT | N,N 767 | XP_005268480.1 | |
XM_011537637.2 | 2790 | Silent Mutation | AAC,AAT | N,N 369 | XP_011535939.1 | |
XM_017009397.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | XP_016864886.1 | |
XM_017009398.1 | 2790 | Silent Mutation | AAC,AAT | N,N 766 | XP_016864887.1 |
Set Membership: |
HapMap DME Validated Inventoried |