Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616197 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
NOL10 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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NOL10 - nucleolar protein 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001261392.1 | 1637 | Silent Mutation | CTA,CTG | L,L 636 | NP_001248321.1 | |
NM_001261394.1 | 1637 | Silent Mutation | CTA,CTG | L,L 612 | NP_001248323.1 | |
NM_024894.3 | 1637 | Silent Mutation | CTA,CTG | L,L 662 | NP_079170.2 | |
XM_011510398.2 | 1637 | Silent Mutation | CTA,CTG | L,L 512 | XP_011508700.1 | |
XM_011510399.2 | 1637 | Silent Mutation | CTA,CTG | L,L 512 | XP_011508701.1 | |
XM_011510400.2 | 1637 | Intron | XP_011508702.1 | |||
XM_011510402.2 | 1637 | Intron | XP_011508704.1 | |||
XM_017004990.1 | 1637 | Silent Mutation | CTA,CTG | L,L 337 | XP_016860479.1 | |
XM_017004991.1 | 1637 | Silent Mutation | CTA,CTG | L,L 337 | XP_016860480.1 |