Product Details

SNP ID
rs77776961
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:116087571 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACGGTTGCTCACTCGGATTCTTC[A/C]AAAACTTCACCTGAAGGTTTGTATT
Phenotype
MIM: 616704
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
COMMD10 PubMed Links

Gene Details

Gene
COMMD10
Gene Name
COMM domain containing 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308080.1 577 Missense Mutation CAA,CCA Q25P NP_001295009.1
NM_016144.3 577 Missense Mutation CAA,CCA Q39P NP_057228.1
XM_011543458.2 577 Missense Mutation CAA,CCA Q39P XP_011541760.1
XM_011543460.2 577 Missense Mutation CAA,CCA Q39P XP_011541762.1
XM_017009553.1 577 Missense Mutation CAA,CCA Q25P XP_016865042.1
XM_017009555.1 577 Missense Mutation CAA,CCA Q39P XP_016865044.1
XM_017009556.1 577 Missense Mutation CAA,CCA Q39P XP_016865045.1
XM_017009557.1 577 Intron XP_016865046.1

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