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ATCCCGGCCCAGTGGGATGCCAAAA[C/T]GACGGAGAGCCACATCTCTGATCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612088 MIM: 606783 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLEC12A 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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CLEC12A - C-type lectin domain family 12 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001207010.1 | Intron | NP_001193939.1 | ||||
NM_001300730.1 | Intron | NP_001287659.1 | ||||
NM_138337.5 | Intron | NP_612210.4 | ||||
NM_201623.3 | Intron | NP_963917.2 | ||||
XM_005253324.2 | Intron | XP_005253381.1 | ||||
XM_006719033.3 | Intron | XP_006719096.1 | ||||
XM_006719035.3 | Intron | XP_006719098.1 | ||||
XM_006719036.3 | Intron | XP_006719099.1 | ||||
XM_011520570.1 | Intron | XP_011518872.1 | ||||
XM_011520571.2 | Intron | XP_011518873.2 | ||||
XM_011520573.2 | Intron | XP_011518875.1 |
CLEC1B - C-type lectin domain family 1 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099431.1 | Intron | NP_001092901.1 | ||||
NM_016509.3 | Intron | NP_057593.3 | ||||
XM_005253382.4 | Intron | XP_005253439.1 | ||||
XM_011520685.2 | Intron | XP_011518987.1 | ||||
XM_011520686.2 | Intron | XP_011518988.1 | ||||
XM_017019395.1 | Intron | XP_016874884.1 | ||||
XM_017019396.1 | Intron | XP_016874885.1 |