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TCTGGATGTGTACATGCAGGTCATA[A/G]GCATATACACAGGCATATGATGGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 612088 | ||||||||||||||||||||
Literature Links: |
CLEC12A 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 |
CLEC12A - C-type lectin domain family 12 member A | ||||||
---|---|---|---|---|---|---|
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 |