Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCACCTCAAGCCTCTGCAGATAG[C/G]TGAGCTCCTGCAGGCCAGCATCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609079 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FBXL12 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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FBXL12 - F-box and leucine rich repeat protein 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316936.1 | 895 | Missense Mutation | ACC,AGC | T,S 169 | NP_001303865.1 | |
NM_001316937.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303866.1 | |
NM_001316938.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303867.1 | |
NM_001316939.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303868.1 | |
NM_001316940.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303869.1 | |
NM_001316941.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303870.1 | |
NM_001316942.1 | 895 | Missense Mutation | ACC,AGC | T,S 149 | NP_001303871.1 | |
NM_017703.2 | 895 | Missense Mutation | ACC,AGC | T,S 202 | NP_060173.1 | |
XM_006722782.3 | 895 | Missense Mutation | ACC,AGC | T,S 160 | XP_006722845.2 | |
XM_017026912.1 | 895 | Missense Mutation | ACC,AGC | T,S 219 | XP_016882401.1 |