Product Details

SNP ID: rs147620158
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829797 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGAGGGTACTCGGTGCAGCTGGAC[A/G]CTCTGCACTTCTCGACTTTCGAGGA
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	871	Missense Mutation	ACT,GCT	T291A	NP_005163.1