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SAT2
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611463
MIM: 182205
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Literature Links: |
SAT2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
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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| SAT2 - spermidine/spermine N1-acetyltransferase family member 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| SHBG - sex hormone binding globulin | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001040.4 | 892 | Silent Mutation | TCC,TCT | S,S 289 | NP_001031.2 | |
| NM_001146279.2 | 892 | Silent Mutation | TCC,TCT | S,S 271 | NP_001139751.1 | |
| NM_001146280.2 | 892 | Intron | NP_001139752.1 | |||
| NM_001146281.2 | 892 | Intron | NP_001139753.1 | |||
| NM_001289113.1 | 892 | Silent Mutation | TCC,TCT | S,S 231 | NP_001276042.1 | |
| NM_001289114.1 | 892 | Silent Mutation | TCC,TCT | S,S 231 | NP_001276043.1 | |
| NM_001289115.1 | 892 | Intron | NP_001276044.1 | |||
| NM_001289116.1 | 892 | Silent Mutation | TCC,TCT | S,S 173 | NP_001276045.1 | |
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