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CTAATGTAACCAAATTCCCAAATCC[A/C]ATTCTGAGGCTCTCCATGTCAAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604591 MIM: 616711 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PEBP1 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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PEBP1 - phosphatidylethanolamine binding protein 1 | ||||||
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There are no transcripts associated with this gene. |
TAOK3 - TAO kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016281.3 | 3470 | Missense Mutation | ATG,ATT | M,I 882 | NP_057365.3 | |
XM_005253897.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_005253954.1 | |
XM_005253898.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_005253955.1 | |
XM_006719445.2 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_006719508.1 | |
XM_011538437.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_011536739.1 | |
XM_011538439.1 | 3470 | Missense Mutation | ATG,ATT | M,I 882 | XP_011536741.1 | |
XM_017019408.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_016874897.1 | |
XM_017019409.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_016874898.1 | |
XM_017019410.1 | 3470 | Missense Mutation | ATG,ATT | M,I 891 | XP_016874899.1 | |
XM_017019411.1 | 3470 | Missense Mutation | ATG,ATT | M,I 882 | XP_016874900.1 | |
XM_017019412.1 | 3470 | Missense Mutation | ATG,ATT | M,I 721 | XP_016874901.1 | |
XM_017019413.1 | 3470 | Missense Mutation | ATG,ATT | M,I 712 | XP_016874902.1 |