Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGCTGTCAGAGGGTGTGGCAGGCG[A/G]TCTCAGGCACACCGGGGAACTGAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609093 | ||||||||||||||||||||
Literature Links: |
FBXO15 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 |
FBXO15 - F-box protein 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142958.1 | 1435 | Missense Mutation | CCG,TCG | P,S 449 | NP_001136430.1 | |
NM_152676.2 | 1435 | Missense Mutation | CCG,TCG | P,S 373 | NP_689889.1 | |
XM_011525856.1 | 1435 | Missense Mutation | CCG,TCG | P,S 379 | XP_011524158.1 | |
XM_011525858.2 | 1435 | Intron | XP_011524160.1 | |||
XM_011525859.1 | 1435 | Intron | XP_011524161.1 | |||
XM_011525860.1 | 1435 | Intron | XP_011524162.1 | |||
XM_017025603.1 | 1435 | Missense Mutation | CCG,TCG | P,S 373 | XP_016881092.1 | |
XM_017025604.1 | 1435 | Missense Mutation | CCG,TCG | P,S 373 | XP_016881093.1 |