Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTTACCCGTGTTGTGTCTCCCTCC[C/T]GCTTAATCATATCCATTCCAGGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 601993 | ||||||||||||||||||||
Literature Links: |
NCOA2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NCOA2 - nuclear receptor coactivator 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321703.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1455 | NP_001308632.1 | |
NM_001321707.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1455 | NP_001308636.1 | |
NM_001321711.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1386 | NP_001308640.1 | |
NM_001321712.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1386 | NP_001308641.1 | |
NM_001321713.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1301 | NP_001308642.1 | |
NM_006540.3 | 4828 | Missense Mutation | CAG,CGG | Q,R 1455 | NP_006531.1 | |
XM_017012961.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868450.1 | |
XM_017012962.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868451.1 | |
XM_017012963.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868452.1 | |
XM_017012964.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868453.1 | |
XM_017012965.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868454.1 | |
XM_017012966.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868455.1 | |
XM_017012967.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868456.1 | |
XM_017012968.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868457.1 | |
XM_017012969.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868458.1 | |
XM_017012970.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868459.1 | |
XM_017012971.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1524 | XP_016868460.1 | |
XM_017012972.1 | 4828 | Missense Mutation | CAG,CGG | Q,R 1370 | XP_016868461.1 | |
XM_017012973.1 | 4828 | Intron | XP_016868462.1 |