Product Details

SNP ID
rs9905879
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:61412461 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCAGCGAGTCCTCTTGGCAGCTCCC[A/G]CAGCTCCCCGCCGGGAGCACGAGTG
Phenotype
MIM: 600747
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
C17orf82 PubMed Links

Gene Details

Gene
C17orf82
Gene Name
chromosome 17 open reading frame 82
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_203425.2 711 Silent Mutation CCA,CCG P162P NP_982249.2
Gene
TBX2
Gene Name
T-box 2
There are no transcripts associated with this gene.

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