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AGGGCCGGCCGGAGCTCCAGGATGC[A/G]CTCGGCCCGGCCCAGGTGTGAGAGG
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 | 8304 | Missense Mutation | CGC,TGC | R,C 2722 | NP_001308360.1 | |
NM_032447.4 | 8304 | Missense Mutation | CGC,TGC | R,C 2722 | NP_115823.3 | |
XM_017027372.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2722 | XP_016882861.1 | |
XM_017027373.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2702 | XP_016882862.1 | |
XM_017027374.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2690 | XP_016882863.1 | |
XM_017027375.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2681 | XP_016882864.1 | |
XM_017027376.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2679 | XP_016882865.1 | |
XM_017027377.1 | 8304 | Missense Mutation | CGC,TGC | R,C 1861 | XP_016882866.1 | |
XM_017027378.1 | 8304 | Missense Mutation | CGC,TGC | R,C 1508 | XP_016882867.1 | |
XM_017027379.1 | 8304 | Missense Mutation | CGC,TGC | R,C 2764 | XP_016882868.1 |