Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGTTCTTCATGTACCTCTGGACCC[A/C]CTCCTGCTTGGGGTCGCCACAGAAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 602495 | ||||||||||||||||||||
Literature Links: |
CCL24 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
CCL24 - C-C motif chemokine ligand 24 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002991.2 | 508 | Missense Mutation | GGG,TGG | G,W 81 | NP_002982.2 | |
XM_011516459.2 | 508 | Missense Mutation | GGG,TGG | G,W 81 | XP_011514761.1 | |
XM_011516460.2 | 508 | Missense Mutation | GGG,TGG | G,W 81 | XP_011514762.1 |