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TCCGCGGACGATGACGTAGCGGATC[C/T]GGCCCTCTAGACCCTCCAGGGCCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602565 MIM: 608529 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCL25 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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CCL25 - C-C motif chemokine ligand 25 | ||||||
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There are no transcripts associated with this gene. |
FBN3 - fibrillin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321431.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2736 | NP_001308360.1 | |
NM_032447.4 | 8347 | Missense Mutation | CAG,CGG | Q,R 2736 | NP_115823.3 | |
XM_017027372.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2736 | XP_016882861.1 | |
XM_017027373.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2716 | XP_016882862.1 | |
XM_017027374.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2704 | XP_016882863.1 | |
XM_017027375.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2695 | XP_016882864.1 | |
XM_017027376.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2693 | XP_016882865.1 | |
XM_017027377.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 1875 | XP_016882866.1 | |
XM_017027378.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 1522 | XP_016882867.1 | |
XM_017027379.1 | 8347 | Missense Mutation | CAG,CGG | Q,R 2778 | XP_016882868.1 |