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Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615769 MIM: 606544 MIM: 612497 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM169A 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)
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EUR
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AMR
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FAM169A - family with sequence similarity 169 member A | ||||||
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There are no transcripts associated with this gene. |
GFM2 - G elongation factor mitochondrial 2 | ||||||
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There are no transcripts associated with this gene. |
NSA2 - NSA2, ribosome biogenesis homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271665.1 | 401 | Missense Mutation | CGT,TGT | R,C 11 | NP_001258594.1 | |
NM_014886.4 | 401 | Missense Mutation | CGT,TGT | R,C 11 | NP_055701.1 | |
XM_011543098.1 | 401 | Intron | XP_011541400.1 | |||
XM_017008952.1 | 401 | Intron | XP_016864441.1 | |||
XM_017008953.1 | 401 | Intron | XP_016864442.1 |