Product Details

SNP ID
rs4340196
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:75526276 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCATCCAGTACAAGTTTTTAAACTA[C/T]TGTTGTAACACATAAATTTGTGCTG
Phenotype
MIM: 612377
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
COMMD6 PubMed Links

Gene Details

Gene
COMMD6
Gene Name
COMM domain containing 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287392.1 677 UTR 3 NP_001274321.1
NM_001287393.1 677 UTR 3 NP_001274322.1
NM_001287394.1 677 UTR 3 NP_001274323.1
NM_203495.3 677 UTR 3 NP_987091.1
NM_203497.3 677 UTR 3 NP_987093.1
XM_011534948.2 677 Intron XP_011533250.1

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