Product Details

SNP ID

rs201848347

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:57360476 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AACATGGAAGACAGCGTCTGCTGCC[A/G]TGATTACGTCCGTTACCGTCTGCCC

Phenotype

MIM: 602957

Polymorphism

A/G, 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	167	Missense Mutation	CAT,CGT	H38R	NP_002981.2
XM_017023531.1	167	Missense Mutation	CAT,CGT	H38R	XP_016879020.1

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