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AGCTGACGCCACGGAGGTGATGCAT[A/G]CGAAAGAAACCTTGCTCGTTTCCGC
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 |
---|---|---|
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 |
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 | 8393 | Silent Mutation | CGC,CGT | R,R 2751 | NP_001308360.1 | |
NM_032447.4 | 8393 | Silent Mutation | CGC,CGT | R,R 2751 | NP_115823.3 | |
XM_017027372.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2751 | XP_016882861.1 | |
XM_017027373.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2731 | XP_016882862.1 | |
XM_017027374.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2719 | XP_016882863.1 | |
XM_017027375.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2710 | XP_016882864.1 | |
XM_017027376.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2708 | XP_016882865.1 | |
XM_017027377.1 | 8393 | Silent Mutation | CGC,CGT | R,R 1890 | XP_016882866.1 | |
XM_017027378.1 | 8393 | Silent Mutation | CGC,CGT | R,R 1537 | XP_016882867.1 | |
XM_017027379.1 | 8393 | Silent Mutation | CGC,CGT | R,R 2793 | XP_016882868.1 |