Product Details

SNP ID

rs147844594

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:57360545 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCTACTGGACCTCAGACTCCTGCC[C/T]GAGGCCTGGCGTGGTGTGAGTAGGG

Phenotype

MIM: 602957

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CCL22 PubMed Links

Gene Details

Gene

CCL22

Gene Name

C-C motif chemokine ligand 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002990.4	236	Missense Mutation	CCG,CTG	P61L	NP_002981.2
XM_017023531.1	236	Missense Mutation	CCG,CTG	P61L	XP_016879020.1

View Full Product Details