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GGATTCTGCTGGAGCAAGGAATAAC[C/T]GAGATGGAAATAACCTAAGAAAAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606783 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLEC12B 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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CLEC12B - C-type lectin domain family 12 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001129998.2 | 288 | Nonsense Mutation | CGA,TGA | R,* 22 | NP_001123470.1 | |
NM_001319241.1 | 288 | UTR 5 | NP_001306170.1 | |||
NM_001319242.1 | 288 | UTR 5 | NP_001306171.1 | |||
NM_205852.3 | 288 | Nonsense Mutation | CGA,TGA | R,* 22 | NP_995324.2 | |
XM_011520658.2 | 288 | Nonsense Mutation | CGA,TGA | R,* 13 | XP_011518960.1 | |
XM_011520663.2 | 288 | Nonsense Mutation | CGA,TGA | R,* 22 | XP_011518965.1 | |
XM_017019295.1 | 288 | UTR 5 | XP_016874784.1 |
CLEC1B - C-type lectin domain family 1 member B | ||||||
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There are no transcripts associated with this gene. |
LOC102724020 - uncharacterized LOC102724020 | ||||||
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There are no transcripts associated with this gene. |