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CAGTGCAGCCCTCCAGGATGATGAC[A/G]CCCACGGGCTCACGGCTGGCAGCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614239 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM109A 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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FAM109A - family with sequence similarity 109 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177996.1 | 568 | Silent Mutation | GGC,GGT | G,G 72 | NP_001171467.1 | |
NM_001177997.1 | 568 | Silent Mutation | GGC,GGT | G,G 59 | NP_001171468.1 | |
NM_144671.4 | 568 | Silent Mutation | GGC,GGT | G,G 59 | NP_653272.2 | |
XM_006719257.3 | 568 | Silent Mutation | GGC,GGT | G,G 59 | XP_006719320.1 | |
XM_011537976.2 | 568 | Silent Mutation | GGC,GGT | G,G 59 | XP_011536278.1 | |
XM_017018883.1 | 568 | Silent Mutation | GGC,GGT | G,G 59 | XP_016874372.1 |