Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 126063 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
DLST 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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DLST - dihydrolipoamide S-succinyltransferase | ||||||
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There are no transcripts associated with this gene. |
RPS6KL1 - ribosomal protein S6 kinase like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_031464.4 | 1861 | UTR 3 | NP_113652.2 | |||
XM_011537206.2 | 1861 | Missense Mutation | CTC,TTC | L,F 596 | XP_011535508.1 | |
XM_011537207.2 | 1861 | Missense Mutation | CTC,TTC | L,F 596 | XP_011535509.1 | |
XM_011537211.2 | 1861 | Missense Mutation | CTC,TTC | L,F 549 | XP_011535513.1 | |
XM_011537213.2 | 1861 | Missense Mutation | CTC,TTC | L,F 533 | XP_011535515.1 | |
XM_017021680.1 | 1861 | Missense Mutation | CTC,TTC | L,F 596 | XP_016877169.1 | |
XM_017021681.1 | 1861 | Missense Mutation | CTC,TTC | L,F 580 | XP_016877170.1 | |
XM_017021682.1 | 1861 | Missense Mutation | CTC,TTC | L,F 580 | XP_016877171.1 | |
XM_017021683.1 | 1861 | Missense Mutation | CTC,TTC | L,F 566 | XP_016877172.1 | |
XM_017021684.1 | 1861 | Missense Mutation | CTC,TTC | L,F 564 | XP_016877173.1 | |
XM_017021685.1 | 1861 | Intron | XP_016877174.1 | |||
XM_017021686.1 | 1861 | Intron | XP_016877175.1 | |||
XM_017021687.1 | 1861 | Intron | XP_016877176.1 | |||
XM_017021688.1 | 1861 | Missense Mutation | CTC,TTC | L,F 394 | XP_016877177.1 | |
XM_017021689.1 | 1861 | Intron | XP_016877178.1 | |||
XM_017021690.1 | 1861 | Intron | XP_016877179.1 | |||
XM_017021691.1 | 1861 | Missense Mutation | CTC,TTC | L,F 317 | XP_016877180.1 | |
XM_017021692.1 | 1861 | Intron | XP_016877181.1 |
Set Membership: |
HapMap |