Product Details

SNP ID
rs78651819
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:35043186 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGAGGCACAAGATAGCATCAGGGA[A/C]CCGCCAGCAGCAGAGAAAAAGCCAG
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
C9orf131 PubMed Links

Gene Details

Gene
C9orf131
Gene Name
chromosome 9 open reading frame 131
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040410.2 388 Missense Mutation AAC,ACC N151T NP_001035500.1
NM_001040411.2 388 Missense Mutation AAC,ACC N113T NP_001035501.1
NM_001040412.2 388 Missense Mutation AAC,ACC N138T NP_001035502.1
NM_001287391.1 388 Missense Mutation AAC,ACC N113T NP_001274320.1
NM_203299.3 388 Missense Mutation AAC,ACC N186T NP_976044.2

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