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GCACCCCCTCGCCCCCCGAAGACCC[C/T]GACTGCCCCCGCGCCTTCGTGTCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605299 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCOA6 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NCOA6 - nuclear receptor coactivator 6 | ||||||
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There are no transcripts associated with this gene. |
TP53INP2 - tumor protein p53 inducible nuclear protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005260476.2 | 25 | Silent Mutation | CCC,CCT | P,P 19 | XP_005260533.1 | |
XM_006723841.2 | 25 | UTR 5 | XP_006723904.1 | |||
XM_011528952.2 | 25 | Silent Mutation | CCC,CCT | P,P 19 | XP_011527254.1 | |
XM_011528953.2 | 25 | Silent Mutation | CCC,CCT | P,P 19 | XP_011527255.1 |