Product Details

SNP ID: rs145666261
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829728 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTCCGGAGGGAGCCAGCGGCCGACC[C/T]CGCCCGGGAGTTGCCGGACTCGCTT
Phenotype: MIM: 601461
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ATOH1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005172.1	802	Missense Mutation	CCG,TCG	P268S	NP_005163.1