Product Details

SNP ID
rs199643997
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:16067689 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGACTCTCCCCGGCTGCTTTCTT[C/T]GATGTCTGTGGCTTTGTCATAATTT
Phenotype
MIM: 613338
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MARCH11 PubMed Links

Gene Details

Gene
MARCH11
Gene Name
membrane associated ring-CH-type finger 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001102562.1 1204 Missense Mutation AAA,GAA K331E NP_001096032.1

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