Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTCCTCAGCCAAGGAAATAAAAAGC[A/C]ACAAAATAGAAAAGAAAAAGAAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LARP1B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LARP1B - La ribonucleoprotein domain family member 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278604.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | NP_001265533.1 | |
NM_018078.3 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | NP_060548.2 | |
NM_032239.3 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | NP_115615.2 | |
NM_178043.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | NP_835144.1 | |
XM_011532057.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530359.2 | |
XM_011532058.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530360.2 | |
XM_011532059.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530361.2 | |
XM_011532060.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530362.2 | |
XM_011532061.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530363.1 | |
XM_011532062.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530364.2 | |
XM_011532063.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530365.2 | |
XM_011532064.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530366.2 | |
XM_011532065.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530367.1 | |
XM_011532067.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_011530369.1 | |
XM_011532068.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_011530370.1 | |
XM_011532069.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_011530371.1 | |
XM_011532070.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530372.2 | |
XM_011532072.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530374.2 | |
XM_011532073.2 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_011530375.2 | |
XM_011532075.1 | 1082 | UTR 5 | XP_011530377.1 | |||
XM_011532076.2 | 1082 | UTR 5 | XP_011530378.1 | |||
XM_011532077.2 | 1082 | Intron | XP_011530379.1 | |||
XM_017008338.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863827.1 | |
XM_017008339.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863828.1 | |
XM_017008340.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_016863829.1 | |
XM_017008341.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_016863830.1 | |
XM_017008342.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 13 | XP_016863831.1 | |
XM_017008343.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_016863832.1 | |
XM_017008344.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_016863833.1 | |
XM_017008345.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863834.1 | |
XM_017008346.1 | 1082 | UTR 5 | XP_016863835.1 | |||
XM_017008347.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863836.1 | |
XM_017008348.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863837.1 | |
XM_017008349.1 | 1082 | UTR 5 | XP_016863838.1 | |||
XM_017008350.1 | 1082 | Intron | XP_016863839.1 | |||
XM_017008351.1 | 1082 | UTR 5 | XP_016863840.1 | |||
XM_017008352.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 227 | XP_016863841.1 | |
XM_017008353.1 | 1082 | Missense Mutation | CAA,CCA | Q,P 26 | XP_016863842.1 |