Product Details

SNP ID
rs181176366
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:85754736 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCGGAGTCCACTGTGCGCCCTGCG[C/G]CCCCGACGCGCCCCGGGGAAAGTTC
Phenotype
Polymorphism
C/G, 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_032827.6 951 Missense Mutation CCC,GCC P183A NP_116216.2
XM_006712122.3 951 Missense Mutation CCC,GCC P183A XP_006712185.1
XM_011533139.1 951 Missense Mutation CCC,GCC P183A XP_011531441.1

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