Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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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 | 1768 | Intron | NP_001244956.1 | |||
NM_001321308.1 | 1768 | Intron | NP_001308237.1 | |||
NM_173535.2 | 1768 | Missense Mutation | AAG,AGG | K,R 564 | NP_775806.2 | |
XM_011532635.2 | 1768 | Missense Mutation | AAG,AGG | K,R 674 | XP_011530937.1 | |
XM_011532637.2 | 1768 | Missense Mutation | AAG,AGG | K,R 674 | XP_011530939.1 | |
XM_011532638.2 | 1768 | Intron | XP_011530940.1 | |||
XM_011532639.2 | 1768 | Intron | XP_011530941.1 | |||
XM_011532640.2 | 1768 | Intron | XP_011530942.1 | |||
XM_011532641.2 | 1768 | Intron | XP_011530943.1 | |||
XM_011532642.2 | 1768 | Missense Mutation | AAG,AGG | K,R 534 | XP_011530944.1 | |
XM_011532643.1 | 1768 | Missense Mutation | AAG,AGG | K,R 503 | XP_011530945.1 | |
XM_017003519.1 | 1768 | Missense Mutation | AAG,AGG | K,R 674 | XP_016859008.1 |
Set Membership: |
HapMap |