Product Details

SNP ID
rs147689299
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.7:77196933 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGTAACTCTGTAGGTCTCACTGCT[G/T]CTTTTGCCTATTGCGTAGTAGTCAG
Phenotype
MIM: 605351
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
CCDC146 PubMed Links

Gene Details

Gene
CCDC146
Gene Name
coiled-coil domain containing 146
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020879.2 706 Intron NP_065930.2
Gene
FGL2
Gene Name
fibrinogen like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_006682.2 706 Missense Mutation NP_006673.1

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