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TCCAGCTATGTGTTTTATTGGCGGG[A/G]TTACTTTGAGGACCAGCCCCTTCTG
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 |
---|---|---|
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 |
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 | 480 | Intron | NP_001304753.1 | |||
NM_001317825.1 | 480 | Missense Mutation | GAT,GGT | D,G 18 | NP_001304754.1 | |
NM_001317826.1 | 480 | Missense Mutation | GAT,GGT | D,G 81 | NP_001304755.1 | |
NM_017872.4 | 480 | Missense Mutation | GAT,GGT | D,G 143 | NP_060342.2 | |
XM_017009603.1 | 480 | Intron | XP_016865092.1 |