Product Details

SNP ID
rs4921056
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:116087237 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGCTCTTCCCTGCGCAGTACAAGG[C/T]TTCCCTAGTAGTTTGGTTTGCCCAA
Phenotype
MIM: 616704
Polymorphism
C/T, Transition 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 Intron NP_001295009.1
NM_016144.3 Intron NP_057228.1
XM_011543458.2 Intron XP_011541760.1
XM_011543460.2 Intron XP_011541762.1
XM_017009553.1 Intron XP_016865042.1
XM_017009555.1 Intron XP_016865044.1
XM_017009556.1 Intron XP_016865045.1
XM_017009557.1 Intron XP_016865046.1

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