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CAACGGTCCATCTGAGGATGTAGGT[A/T]GGCCGGATCCCGCTGATCCCCAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300964 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAS1L 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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LAS1L - LAS1 like, ribosome biogenesis factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170649.1 | 1273 | Silent Mutation | CCA,CCT | P,P 399 | NP_001164120.1 | |
NM_001170650.1 | 1273 | Silent Mutation | CCA,CCT | P,P 357 | NP_001164121.1 | |
NM_031206.4 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | NP_112483.1 | |
XM_005262301.1 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | XP_005262358.1 | |
XM_005262304.1 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | XP_005262361.1 | |
XM_005262305.3 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | XP_005262362.1 | |
XM_005262306.3 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | XP_005262363.1 | |
XM_011531045.1 | 1273 | Silent Mutation | CCA,CCT | P,P 374 | XP_011529347.1 | |
XM_011531046.1 | 1273 | Silent Mutation | CCA,CCT | P,P 416 | XP_011529348.1 | |
XM_017029877.1 | 1273 | Silent Mutation | CCA,CCT | P,P 399 | XP_016885366.1 | |
XM_017029878.1 | 1273 | Silent Mutation | CCA,CCT | P,P 399 | XP_016885367.1 | |
XM_017029879.1 | 1273 | Silent Mutation | CCA,CCT | P,P 114 | XP_016885368.1 | |
XM_017029880.1 | 1273 | Silent Mutation | CCA,CCT | P,P 97 | XP_016885369.1 |