Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCGGATCTTGCGCACATCTCGGA[C/G]GTGGCGGCTGATGGCCAGCAGGGTG
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 |
---|---|---|
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 |
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 | 969 | Missense Mutation | CTC,GTC | L,V 194 | NP_001303865.1 | |
NM_001316937.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303866.1 | |
NM_001316938.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303867.1 | |
NM_001316939.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303868.1 | |
NM_001316940.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303869.1 | |
NM_001316941.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303870.1 | |
NM_001316942.1 | 969 | Missense Mutation | CTC,GTC | L,V 174 | NP_001303871.1 | |
NM_017703.2 | 969 | Missense Mutation | CTC,GTC | L,V 227 | NP_060173.1 | |
XM_006722782.3 | 969 | Missense Mutation | CTC,GTC | L,V 185 | XP_006722845.2 | |
XM_017026912.1 | 969 | Missense Mutation | CTC,GTC | L,V 244 | XP_016882401.1 |