Product Details

SNP ID: rs111699024
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:68231485 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCTGGCCCCACTGGGGAACCACCC[C/T]GCGTAAGCGGTCGAAGGCAGTGTTG
Phenotype: MIM: 609875
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ATOH7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_145178.3	629	Silent Mutation			NP_660161.1