Product Details

SNP ID: rs146898613
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:68231285 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTCTCTGGCTGTACAGCTCGCTCTC[G/T]CCCGGCAGCTTCGCGCCCGGGAACG
Phenotype: MIM: 609875
Polymorphism: G/T, 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	829	Silent Mutation	GGA,GGC	G131G	NP_660161.1