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GTACACTTTACTTGTGAACTCTACC[A/G]GAAATGCCTGCAGAGAAAAGGCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CLEC4F 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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CLEC4F - C-type lectin domain family 4 member F | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258027.1 | 1624 | Missense Mutation | CCG,CTG | P,L 516 | NP_001244956.1 | |
NM_001321308.1 | 1624 | Missense Mutation | CCG,CTG | P,L 516 | NP_001308237.1 | |
NM_173535.2 | 1624 | Missense Mutation | CCG,CTG | P,L 516 | NP_775806.2 | |
XM_011532635.2 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_011530937.1 | |
XM_011532637.2 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_011530939.1 | |
XM_011532638.2 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_011530940.1 | |
XM_011532639.2 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_011530941.1 | |
XM_011532640.2 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_011530942.1 | |
XM_011532641.2 | 1624 | Silent Mutation | TCC,TCT | S,S 575 | XP_011530943.1 | |
XM_011532642.2 | 1624 | Missense Mutation | CCG,CTG | P,L 486 | XP_011530944.1 | |
XM_011532643.1 | 1624 | Missense Mutation | CCG,CTG | P,L 455 | XP_011530945.1 | |
XM_017003519.1 | 1624 | Missense Mutation | CCG,CTG | P,L 626 | XP_016859008.1 |