Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611463 MIM: 182205 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SAT2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SAT2 - spermidine/spermine N1-acetyltransferase family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320845.1 | 634 | Missense Mutation | CGC,TGC | R,C 205 | NP_001307774.1 | |
NM_001320846.1 | 634 | Missense Mutation | CGC,TGC | R,C 171 | NP_001307775.1 | |
NM_001320847.1 | 634 | Missense Mutation | CGC,TGC | R,C 92 | NP_001307776.1 | |
NM_133491.4 | 634 | Missense Mutation | CGC,TGC | R,C 126 | NP_597998.1 | |
XM_017024073.1 | 634 | UTR 3 | XP_016879562.1 | |||
XM_017024074.1 | 634 | UTR 3 | XP_016879563.1 |
SHBG - sex hormone binding globulin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040.4 | 634 | Intron | NP_001031.2 | |||
NM_001146279.2 | 634 | Intron | NP_001139751.1 | |||
NM_001146280.2 | 634 | Intron | NP_001139752.1 | |||
NM_001146281.2 | 634 | Intron | NP_001139753.1 | |||
NM_001289113.1 | 634 | Intron | NP_001276042.1 | |||
NM_001289114.1 | 634 | Intron | NP_001276043.1 | |||
NM_001289115.1 | 634 | Intron | NP_001276044.1 | |||
NM_001289116.1 | 634 | Intron | NP_001276045.1 |
Set Membership: |
HapMap |