Product Details

SNP ID

rs150951637

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:75771899 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGAGAAATACTCACATCACAGCCC[A/G]CTGGGAGCAGCTGTTACTGGTGAAT

Phenotype

MIM: 604697

Polymorphism

A/G, Transition 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	372	Missense Mutation	CGG,TGG	R60W	NP_006063.1
XM_017011671.1	372	Missense Mutation	CGG,TGG	R114W	XP_016867160.1
XM_017011672.1	372	Missense Mutation	CGG,TGG	R60W	XP_016867161.1

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