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CCTGCCACCTGCCTCCTAGGGTCCC[C/T]TGGGACTCATGCATGAGAGCCTCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601624 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FCN2 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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FCN2 - ficolin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004108.2 | Intron | NP_004099.2 | ||||
NM_015837.2 | Intron | NP_056652.1 | ||||
XM_006717015.3 | Intron | XP_006717078.1 | ||||
XM_011518392.2 | Intron | XP_011516694.1 |
LOC101448202 - uncharacterized LOC101448202 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |