Product Details

SNP ID: rs138274069
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:68231503 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACCACCCTGCGTAAGCGGTCGAAGG[C/G]AGTGTTGAGCCCCTGCATGCGGCGG
Phenotype: MIM: 609875
Polymorphism: C/G, Transversion 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	611	Missense Mutation	CCC,GCC	P59A	NP_660161.1