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Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
56 submissions
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Phenotype: |
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Literature Links: |
FAM76A 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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FAM76A - family with sequence similarity 76 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143912.1 | 438 | Silent Mutation | GCA,GCG | A,A 112 | NP_001137384.1 | |
NM_001143913.1 | 438 | Silent Mutation | GCA,GCG | A,A 112 | NP_001137385.1 | |
NM_001143914.1 | 438 | Silent Mutation | GCA,GCG | A,A 78 | NP_001137386.1 | |
NM_001143915.1 | 438 | Intron | NP_001137387.1 | |||
NM_152660.2 | 438 | Silent Mutation | GCA,GCG | A,A 78 | NP_689873.1 | |
XM_017000543.1 | 438 | Silent Mutation | GCA,GCG | A,A 78 | XP_016856032.1 |