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AAGTACAAAAGGGTATGGTGAAAAC[C/T]ATCCTCCTACTCACTCCTTTCTTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609752 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCOA7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
|
NCOA7 - nuclear receptor coactivator 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122842.2 | Intron | NP_001116314.1 | ||||
NM_001199619.1 | Intron | NP_001186548.1 | ||||
NM_001199620.1 | Intron | NP_001186549.1 | ||||
NM_001199621.1 | Intron | NP_001186550.1 | ||||
NM_001199622.1 | Intron | NP_001186551.1 | ||||
NM_181782.4 | Intron | NP_861447.3 | ||||
XM_005266822.4 | Intron | XP_005266879.1 | ||||
XM_006715340.3 | Intron | XP_006715403.1 | ||||
XM_011535455.2 | Intron | XP_011533757.1 | ||||
XM_017010269.1 | Intron | XP_016865758.1 | ||||
XM_017010270.1 | Intron | XP_016865759.1 | ||||
XM_017010271.1 | Intron | XP_016865760.1 | ||||
XM_017010272.1 | Intron | XP_016865761.1 | ||||
XM_017010273.1 | Intron | XP_016865762.1 | ||||
XM_017010274.1 | Intron | XP_016865763.1 |