Product Details

SNP ID
rs35629439
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:35042418 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTATTCGTGGTTTGGCAGATTCAGA[A/G]ATGGTGGCAGCTTGGGAGGTTGCGA
Phenotype
Polymorphism
A/G, Transition 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 70 Intron NP_001035500.1
NM_001040411.2 70 Intron NP_001035501.1
NM_001040412.2 70 Missense Mutation AAA,AGA K7R NP_001035502.1
NM_001287391.1 70 Intron NP_001274320.1
NM_203299.3 70 Missense Mutation AAA,AGA K55R NP_976044.2

View Full Product Details