Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATATCTCCACAGTCTCCCTCCTTGG[C/T]CTCTCGGATCCGCACGGAAGCCATC
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 |
---|---|---|
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 |
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 | 266 | Missense Mutation | GAC,GGC | D,G 82 | NP_001307774.1 | |
NM_001320846.1 | 266 | Missense Mutation | GAC,GGC | D,G 82 | NP_001307775.1 | |
NM_001320847.1 | 266 | Missense Mutation | ACC,GCC | T,A 9 | NP_001307776.1 | |
NM_133491.4 | 266 | Missense Mutation | ACC,GCC | T,A 9 | NP_597998.1 | |
XM_017024073.1 | 266 | Missense Mutation | GAC,GGC | D,G 82 | XP_016879562.1 | |
XM_017024074.1 | 266 | Missense Mutation | GAC,GGC | D,G 82 | 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 | 266 | Intron | NP_001031.2 | |||
NM_001146279.2 | 266 | Intron | NP_001139751.1 | |||
NM_001146280.2 | 266 | Intron | NP_001139752.1 | |||
NM_001146281.2 | 266 | Intron | NP_001139753.1 | |||
NM_001289113.1 | 266 | Intron | NP_001276042.1 | |||
NM_001289114.1 | 266 | Intron | NP_001276043.1 | |||
NM_001289115.1 | 266 | Intron | NP_001276044.1 | |||
NM_001289116.1 | 266 | Intron | NP_001276045.1 |