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