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TAGAGATGTAAGTGTATGTTCTGGA[C/G]GGAGAACGGGTCTCATTCTGGGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605651 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXW11 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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FBXW11 - F-box and WD repeat domain containing 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012300.2 | 1528 | Silent Mutation | CCC,CCG | P,P 533 | NP_036432.2 | |
NM_033644.2 | 1528 | Silent Mutation | CCC,CCG | P,P 520 | NP_387448.2 | |
NM_033645.2 | 1528 | Silent Mutation | CCC,CCG | P,P 499 | NP_387449.2 | |
XM_005265855.4 | 1528 | Silent Mutation | CCC,CCG | P,P 554 | XP_005265912.1 | |
XM_005265856.2 | 1528 | Silent Mutation | CCC,CCG | P,P 522 | XP_005265913.1 | |
XM_005265857.2 | 1528 | Silent Mutation | CCC,CCG | P,P 506 | XP_005265914.1 | |
XM_005265858.2 | 1528 | Silent Mutation | CCC,CCG | P,P 501 | XP_005265915.1 | |
XM_017009279.1 | 1528 | Silent Mutation | CCC,CCG | P,P 533 | XP_016864768.1 | |
XM_017009280.1 | 1528 | Silent Mutation | CCC,CCG | P,P 501 | XP_016864769.1 | |
XM_017009281.1 | 1528 | Silent Mutation | CCC,CCG | P,P 501 | XP_016864770.1 |