Product Details

SNP ID: rs145839632
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829059 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCACCTGCAACTTTGCAGGCGAGA[C/G]AGCATCCCGTCTACCCGCCTGAGCT
Phenotype: MIM: 601461
Polymorphism: C/G, Transversion 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	133	Missense Mutation	CAG,GAG	Q45E	NP_005163.1