Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605625 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYEOV 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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MYEOV - myeloma overexpressed | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001293291.1 | 774 | Missense Mutation | GCG,GTG | A,V 159 | NP_001280220.1 | |
NM_001293294.1 | 774 | Missense Mutation | GCG,GTG | A,V 101 | NP_001280223.1 | |
NM_001293296.1 | 774 | Missense Mutation | GCG,GTG | A,V 101 | NP_001280225.1 | |
NM_001300923.1 | 774 | Missense Mutation | GCG,GTG | A,V 101 | NP_001287852.1 | |
NM_001300924.1 | 774 | Missense Mutation | GCG,GTG | A,V 101 | NP_001287853.1 | |
NM_138768.3 | 774 | Missense Mutation | GCG,GTG | A,V 159 | NP_620123.2 |