Product Details

SNP ID
rs142845673
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:61905705 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCGGCGGGCGAGCTTGAGGGTGG[C/G]AAACCCCTGAGCGGGCTGCTGAATG
Phenotype
MIM: 607238
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
COMMD1 PubMed Links

Gene Details

Gene
COMMD1
Gene Name
copper metabolism domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321781.1 62 Intron NP_001308710.1
NM_001321782.1 62 Intron NP_001308711.1
NM_152516.3 62 Silent Mutation GGC,GGG G9G NP_689729.1
XM_011532558.2 62 Silent Mutation GGC,GGG G9G XP_011530860.1
XM_011532559.2 62 Intron XP_011530861.1
XM_017003412.1 62 Intron XP_016858901.1

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