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AGGATGAAGTGGACGGCTGGCTCAT[A/C]ATTGACCTGCCGGGTGAGGCCTGGG
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 |
---|---|---|
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 |
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 | 79 | Silent Mutation | ATA,ATC | I,I 37 | XP_005260533.1 | |
XM_006723841.2 | 79 | UTR 5 | XP_006723904.1 | |||
XM_011528952.2 | 79 | Silent Mutation | ATA,ATC | I,I 37 | XP_011527254.1 | |
XM_011528953.2 | 79 | Silent Mutation | ATA,ATC | I,I 37 | XP_011527255.1 |