Product Details

SNP ID
rs61752236
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:17738037 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTACATTTCTGGCTAAGCTCCTCA[A/C]GTAGGTGCGTAGGTTCTGGTTAATA
Phenotype
MIM: 601997
Polymorphism
A/C, 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_001196.3 659 Missense Mutation NP_001187.1
NM_001244567.1 659 Missense Mutation NP_001231496.1
NM_001244569.1 659 Missense Mutation NP_001231498.1
NM_001244570.1 659 Missense Mutation NP_001231499.1
NM_001244572.1 659 Missense Mutation NP_001231501.1
NM_197966.2 659 Missense Mutation NP_932070.1
NM_197967.2 659 Missense Mutation NP_932071.1
XM_017028906.1 659 Missense Mutation XP_016884395.1

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