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CTTTGACGGAAGAGTCGTGGTGTAT[A/C]CCAGCAACCAGACTTTAAAGGACTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LSM11 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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LSM11 - LSM11, U7 small nuclear RNA associated | ||||||
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There are no transcripts associated with this gene. |
THG1L - tRNA-histidine guanylyltransferase 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317824.1 | 542 | Missense Mutation | ACC,CCC | T,P 32 | NP_001304753.1 | |
NM_001317825.1 | 542 | Missense Mutation | ACC,CCC | T,P 39 | NP_001304754.1 | |
NM_001317826.1 | 542 | Missense Mutation | ACC,CCC | T,P 102 | NP_001304755.1 | |
NM_017872.4 | 542 | Missense Mutation | ACC,CCC | T,P 164 | NP_060342.2 | |
XM_017009603.1 | 542 | Intron | XP_016865092.1 |