Product Details

SNP ID

hCV11940770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:85754578 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCACGCCGCCGCCGCCGCCGCCTC[C/A]TGCGCCCCAGAGCCAGGCACCTGGG

Phenotype

Polymorphism

C/A, Transversion substitution

Allele Nomenclature

Literature Links

ATOH8 PubMed Links

Gene Details

Gene

ATOH8

Gene Name

atonal bHLH transcription factor 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032827.6	793	Missense Mutation	CAT,CCT	H130P	NP_116216.2

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