Product Details

SNP ID
rs28632120
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:32709634 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGCTCAAAACCCTCTACTATCTC[C/T]TATTTCACTCACAGTAAAATCCAAA
Phenotype
MIM: 616703
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
COMMD7 PubMed Links

Gene Details

Gene
COMMD7
Gene Name
COMM domain containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099339.1 Intron NP_001092809.1
NM_053041.2 Intron NP_444269.2
XM_005260299.3 Intron XP_005260356.1
XM_005260300.3 Intron XP_005260357.1
XM_011528604.2 Intron XP_011526906.1
XM_017027685.1 Intron XP_016883174.1
XM_017027686.1 Intron XP_016883175.1
XM_017027687.1 Intron XP_016883176.1

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