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ATCAGATCGTTCTTCATTTGACATA[A/G]TAGCAACATTGTCTGAACTCCCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615769 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) - Not Available | |||
EUR
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AMR
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FAM169A - family with sequence similarity 169 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015566.2 | 1908 | Missense Mutation | ACT,ATT | T,I 532 | NP_056381.1 | |
XM_005248480.2 | 1908 | Missense Mutation | ACT,ATT | T,I 532 | XP_005248537.1 | |
XM_011543306.2 | 1908 | Missense Mutation | ACT,ATT | T,I 532 | XP_011541608.1 | |
XM_011543307.2 | 1908 | Missense Mutation | ACT,ATT | T,I 532 | XP_011541609.1 | |
XM_017009332.1 | 1908 | Missense Mutation | ACT,ATT | T,I 508 | XP_016864821.1 | |
XM_017009333.1 | 1908 | Missense Mutation | ACT,ATT | T,I 446 | XP_016864822.1 |
NSA2 - NSA2, ribosome biogenesis homolog | ||||||
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There are no transcripts associated with this gene. |