Product Details

SNP ID
rs200732958
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17738131 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTGACTGGCCACCTTCTTGGCCAG[C/G]AGCAGGGCCAGCACCAGCATGGTCT
Phenotype
MIM: 601997
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
BCL2L13 PubMed Links

Gene Details

Gene
BCL2L13
Gene Name
BCL2 like 13
There are no transcripts associated with this gene.

Gene
BID
Gene Name
BH3 interacting domain death agonist
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001196.3 565 Silent Mutation CTC,CTG L154L NP_001187.1
NM_001244567.1 565 Silent Mutation CTC,CTG L154L NP_001231496.1
NM_001244569.1 565 Silent Mutation CTC,CTG L58L NP_001231498.1
NM_001244570.1 565 Silent Mutation CTC,CTG L58L NP_001231499.1
NM_001244572.1 565 Silent Mutation CTC,CTG L58L NP_001231501.1
NM_197966.2 565 Silent Mutation CTC,CTG L200L NP_932070.1
NM_197967.2 565 Silent Mutation CTC,CTG L58L NP_932071.1
XM_017028906.1 565 Silent Mutation CTC,CTG L154L XP_016884395.1

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