Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCCCAGCGGCAGCCCCAGGTCCAG[C/G]GGGGGTCTGGTTGGAGGTCTCTGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 151440 MIM: 164005 MIM: 611669 | ||||||||||||||||||||
Literature Links: |
LYL1 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 |
LYL1 - LYL1, basic helix-loop-helix family member | ||||||
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There are no transcripts associated with this gene. |
NFIX - nuclear factor I X | ||||||
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There are no transcripts associated with this gene. |
TRMT1 - tRNA methyltransferase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136035.2 | 2500 | Missense Mutation | CCT,GCT | P,A 648 | NP_001129507.1 | |
NM_001142554.1 | 2500 | Missense Mutation | CCT,GCT | P,A 619 | NP_001136026.1 | |
NM_017722.3 | 2500 | Missense Mutation | CCT,GCT | P,A 648 | NP_060192.1 | |
XM_006722793.2 | 2500 | Missense Mutation | CCT,GCT | P,A 434 | XP_006722856.1 | |
XM_011528124.1 | 2500 | Missense Mutation | CCT,GCT | P,A 612 | XP_011526426.1 | |
XM_011528125.1 | 2500 | Missense Mutation | CCT,GCT | P,A 434 | XP_011526427.1 | |
XM_017026944.1 | 2500 | Missense Mutation | CCT,GCT | P,A 648 | XP_016882433.1 | |
XM_017026945.1 | 2500 | Missense Mutation | CCT,GCT | P,A 619 | XP_016882434.1 | |
XM_017026946.1 | 2500 | Missense Mutation | CCT,GCT | P,A 405 | XP_016882435.1 | |
XM_017026947.1 | 2500 | Missense Mutation | CCT,GCT | P,A 387 | XP_016882436.1 |