Product Details

SNP ID: rs10897060
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:60430270 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAGAGAGGGAGAGAAAAAAAAAAA[A/C]AACCCGAAGAGATGGAGAGTCCTCT
Phenotype: MIM: 606499
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: MS4A5 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023945.2		Intron			NP_076434.2