Product Details

SNP ID
rs77512031
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:75527843 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGAAAGGAGACTGGAGGTTGCCAG[A/G]AGCTGAGGCTGGGGGTCAATGGGGA
Phenotype
MIM: 612377
Polymorphism
A/G, 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_001287392.1 283 Intron NP_001274321.1
NM_001287393.1 283 Intron NP_001274322.1
NM_001287394.1 283 Intron NP_001274323.1
NM_203495.3 283 Intron NP_987091.1
NM_203497.3 283 Silent Mutation CTC,CTT L72L NP_987093.1
XM_011534948.2 283 Intron XP_011533250.1

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