Product Details

SNP ID: rs34543561
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:93829499 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GCAATGTTATCCCGTCGTTCAACAA[C/T]GACAAGAAGCTGTCCAAATATGAGA
Phenotype: MIM: 601461
Polymorphism: C/T, 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	573	Silent Mutation	AAC,AAT	N191N	NP_005163.1