Product Details

SNP ID: rs149422615
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:74038151 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATGGGGGATGCGGGGTTGAGACAAG[A/C]TTTCTTCCCATTCTTGAGTGTGGCT
Phenotype: MIM: 139111
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: CXCL3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002090.2	412	Missense Mutation	GCT,TCT	A84S	NP_002081.2