Product Details

SNP ID: rs151127788
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:70601130 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAATAAAGATACAGATACATACAG[A/C]CAGCTATGGGAACTTAGAGAAGGAC
Phenotype: MIM: 601259
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: AMBN PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016519.5		Intron			NP_057603.1