Product Details

SNP ID
rs3812766
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:36272502 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATCTGACATCTCTCTCTGCAGGTC[A/G]TGGGGAATGGAAGGAAAGGAGAGGG
Phenotype
MIM: 612299
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
COMMD9 PubMed Links

Gene Details

Gene
COMMD9
Gene Name
COMM domain containing 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001101653.1 2729 UTR 3 NP_001095123.1
NM_001307932.1 2729 UTR 3 NP_001294861.1
NM_001307937.1 2729 UTR 3 NP_001294866.1
NM_014186.3 2729 UTR 3 NP_054905.2
XM_017017625.1 2729 Intron XP_016873114.1

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