Product Details

SNP ID: rs139664764
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829585 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCGAGCTGCTACAAACGCCCAGCG[A/G]AGGGGAACAGCCACCGCCGCCTCCA
Phenotype: MIM: 601461
Polymorphism: A/G, Transition 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	659	Missense Mutation	GAA,GGA	E220G	NP_005163.1