Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAAACATGAGTGACTCCAAGGAACC[A/G]AGGGTGCAGCAGCTGGGCCTCCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605872 | ||||||||||||||||||||
Literature Links: |
CLEC4M 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 |
CLEC4M - C-type lectin domain family 4 member M | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144904.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138376.1 | |
NM_001144905.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138377.1 | |
NM_001144906.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138378.1 | |
NM_001144907.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138379.1 | |
NM_001144908.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138380.1 | |
NM_001144909.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138381.1 | |
NM_001144910.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138382.1 | |
NM_001144911.1 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_001138383.1 | |
NM_014257.4 | 139 | Silent Mutation | CCA,CCG | P,P 7 | NP_055072.3 | |
XM_006722611.2 | 139 | Silent Mutation | CCA,CCG | P,P 7 | XP_006722674.1 | |
XM_006722612.3 | 139 | Silent Mutation | CCA,CCG | P,P 7 | XP_006722675.1 | |
XM_006722613.3 | 139 | Silent Mutation | CCA,CCG | P,P 7 | XP_006722676.1 | |
XM_006722614.3 | 139 | Silent Mutation | CCA,CCG | P,P 7 | XP_006722677.1 | |
XM_006722615.2 | 139 | Silent Mutation | CCA,CCG | P,P 7 | XP_006722678.1 |