Product Details

SNP ID

rs34799130

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:60429700 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGATTCAAGCACCGCACACAGTC[C/T]GGTGTTTCTGGTATTTCCTCCAGAA

Phenotype

MIM: 606499

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MS4A5 PubMed Links

Gene Details

Gene

MS4A5

Gene Name

membrane spanning 4-domains A5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023945.2	112	Missense Mutation	CCG,CTG	P9L	NP_076434.2

View Full Product Details