Product Details

SNP ID
rs41341147
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:75769774 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGATGGGTACAGACTTTCTTGCC[A/T]CTTTTGGTAGTGAATCTGTGAAAAA
Phenotype
MIM: 604697
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
CCL26 PubMed Links

Gene Details

Gene
CCL26
Gene Name
C-C motif chemokine ligand 26
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006072.4 398 Missense Mutation AGA,AGT R68S NP_006063.1
XM_017011671.1 398 Missense Mutation AGA,AGT R122S XP_016867160.1
XM_017011672.1 398 Missense Mutation AGA,AGT R68S XP_016867161.1

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