Product Details

SNP ID
rs6107715
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:5912595 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTAGGATTAATCTTTCAAACTACC[C/T]TGAATCTCAAACAAATGATCTCTGA
Phenotype
MIM: 118920
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CHGB PubMed Links

Gene Details

Gene
CHGB
Gene Name
chromogranin B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001819.2 Intron NP_001810.2

View Full Product Details