Product Details

SNP ID: rs6895604
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.5:135534286 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTAGGCAAGAAACTTGGCGACTTAT[A/T]TTTAGTTTTTATTTACATGAAGCGT
Phenotype: MIM: 601726
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: NEUROG1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006161.2	1664	UTR 3			NP_006152.2