Product Details

SNP ID: hCV27834609
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.10:68232072 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGATGAACTCTTTCCCGAAGCTCA[C/G]GGAAGGAGCGCTTTTAGCGCAGTAG
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	42	UTR 5			NP_660161.1