Product Details

SNP ID: rs149474874
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:68231506 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACCCTGCGTAAGCGGTCGAAGGCAG[C/T]GTTGAGCCCCTGCATGCGGCGGCGC
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	608	Missense Mutation	ACT,GCT	T58A	NP_660161.1