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TTTTCTTGTCTCGGTCTTTGTCCCG[A/G]TCTCGGTCCCTATCTTTGTCTTTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609086 MIM: 604311 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXL20 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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FBXL20 - F-box and leucine rich repeat protein 20 | ||||||
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There are no transcripts associated with this gene. |
MED1 - mediator complex subunit 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004774.3 | 4690 | Silent Mutation | GAC,GAT | D,D 1515 | NP_004765.2 | |
XM_005257465.3 | 4690 | Silent Mutation | GAC,GAT | D,D 1343 | XP_005257522.1 | |
XM_006721957.1 | 4690 | Intron | XP_006722020.1 | |||
XM_017024779.1 | 4690 | Silent Mutation | GAC,GAT | D,D 1296 | XP_016880268.1 |