Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAAACCAAGACCACCTCCTGCTCT[G/T]GGACCGGAGGAGACATCGGCCTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600960 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SET 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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SET - SET nuclear proto-oncogene | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122821.1 | 523 | Silent Mutation | CTG,CTT | L,L 22 | NP_001116293.1 | |
NM_001248000.1 | 523 | Intron | NP_001234929.1 | |||
NM_001248001.1 | 523 | Intron | NP_001234930.1 | |||
NM_003011.3 | 523 | Intron | NP_003002.2 | |||
XM_017015013.1 | 523 | Silent Mutation | CTG,CTT | L,L 22 | XP_016870502.1 | |
XM_017015014.1 | 523 | Intron | XP_016870503.1 | |||
XM_017015015.1 | 523 | Intron | XP_016870504.1 | |||
XM_017015016.1 | 523 | Intron | XP_016870505.1 |