Product Details

SNP ID
rs185077891
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17738091 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCACTGTTGTGTGAAAGACATCAC[A/G]GAGCAAGGACGGCGTGTGACTGGCC
Phenotype
MIM: 601997
Polymorphism
A/G, Transition 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_001196.3 605 Missense Mutation CGT,TGT R168C NP_001187.1
NM_001244567.1 605 Missense Mutation CGT,TGT R168C NP_001231496.1
NM_001244569.1 605 Missense Mutation CGT,TGT R72C NP_001231498.1
NM_001244570.1 605 Missense Mutation CGT,TGT R72C NP_001231499.1
NM_001244572.1 605 Missense Mutation CGT,TGT R72C NP_001231501.1
NM_197966.2 605 Missense Mutation CGT,TGT R214C NP_932070.1
NM_197967.2 605 Missense Mutation CGT,TGT R72C NP_932071.1
XM_017028906.1 605 Missense Mutation CGT,TGT R168C XP_016884395.1

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