Product Details

SNP ID
rs4819616
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17638846 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GACCCTGTCGGAAGCAACTGCCGCC[C/G]CCGCCTCTTTCATCTCTTCTGGGGC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BCL2L13 PubMed Links

Gene Details

Gene
BCL2L13
Gene Name
BCL2 like 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270726.1 263 Silent Mutation CCC,CCG P51P NP_001257655.1
NM_001270727.1 263 Silent Mutation CCC,CCG P51P NP_001257656.1
NM_001270728.1 263 UTR 5 NP_001257657.1
NM_001270729.1 263 UTR 5 NP_001257658.1
NM_001270730.1 263 UTR 5 NP_001257659.1
NM_001270731.1 263 UTR 5 NP_001257660.1
NM_001270732.1 263 UTR 5 NP_001257661.1
NM_001270733.1 263 Intron NP_001257662.1
NM_001270734.1 263 UTR 5 NP_001257663.1
NM_001270735.1 263 UTR 5 NP_001257664.1
NM_015367.3 263 UTR 5 NP_056182.2

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