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TCAAAGTTGATACCTGTGGAAGACA[C/T]AGGCCTCTGGCTAGTCATGTTGCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616825 MIM: 606726 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NCOA5 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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NCOA5 - nuclear receptor coactivator 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020967.2 | 1713 | Missense Mutation | ATG,GTG | M,V 528 | NP_066018.1 | |
XM_005260474.3 | 1713 | Missense Mutation | ATG,GTG | M,V 423 | XP_005260531.1 | |
XM_011528951.2 | 1713 | UTR 3 | XP_011527253.1 | |||
XM_017027988.1 | 1713 | UTR 3 | XP_016883477.1 |
SLC12A5 - solute carrier family 12 member 5 | ||||||
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There are no transcripts associated with this gene. |