Product Details

SNP ID: rs201671383
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829573 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATCAACGCCTTGTCCGAGCTGCTAC[A/G]AACGCCCAGCGGAGGGGAACAGCCA
Phenotype: MIM: 601461
Polymorphism: A/G, 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	647	Missense Mutation	CAA,CGA	Q216R	NP_005163.1