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CGTACGTGTGGCAGTTCCAAGGTGG[C/A]GACTCAGGAGGGAGGCCAGGAGCAC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604697 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCL26 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)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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CCL26 - C-C motif chemokine ligand 26 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006072.4 | 247 | Missense Mutation | CGC,CTC | R,L 18 | NP_006063.1 | |
XM_017011671.1 | 247 | Missense Mutation | CGC,CTC | R,L 72 | XP_016867160.1 | |
XM_017011672.1 | 247 | Missense Mutation | CGC,CTC | R,L 18 | XP_016867161.1 |
Set Membership: |
HapMap |