Product Details

SNP ID
rs185313584
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:8953293 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAACCAGAGTAAGATATACCATGTA[C/G]AGAAGTAGAAGGCCCAAAATGGAGA
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
TMEM9B PubMed Links

Gene Details

Gene
TMEM9B
Gene Name
TMEM9 domain family member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286094.1 811 Silent Mutation CTC,CTG L43L NP_001273023.1
NM_001286095.1 811 Silent Mutation CTC,CTG L43L NP_001273024.1
NM_020644.2 811 Silent Mutation CTC,CTG L117L NP_065695.1

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