Product Details

SNP ID
rs3741400
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64269886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTAGTGAGCACGGCCCCCAGGGCA[C/T]CGCGGGGGCTCGGGTCCCGGTGACG
Phenotype
MIM: 603167 MIM: 600230
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
BAD PubMed Links

Gene Details

Gene
BAD
Gene Name
BCL2 associated agonist of cell death
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004322.3 1166 UTR 3 NP_004313.1
NM_032989.2 1166 UTR 3 NP_116784.1
Gene
GPR137
Gene Name
G protein-coupled receptor 137
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001170726.1 1166 Intron NP_001164197.1
NM_001170880.1 1166 Intron NP_001164351.1
NM_001170881.1 1166 Intron NP_001164352.1
NM_001177358.1 1166 Intron NP_001170829.1
NM_020155.3 1166 Intron NP_064540.3
XM_005274100.2 1166 Intron XP_005274157.1
XM_005274101.2 1166 Intron XP_005274158.1
XM_005274102.2 1166 Intron XP_005274159.1
XM_005274104.2 1166 Intron XP_005274161.1
XM_011545168.2 1166 Intron XP_011543470.1
XM_011545169.1 1166 Intron XP_011543471.1
XM_011545170.2 1166 Intron XP_011543472.1
XM_011545171.2 1166 Intron XP_011543473.1
XM_011545172.2 1166 Intron XP_011543474.1
XM_017018014.1 1166 Intron XP_016873503.1
XM_017018015.1 1166 Intron XP_016873504.1
XM_017018016.1 1166 Intron XP_016873505.1
Gene
PLCB3
Gene Name
phospholipase C beta 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000932.2 1166 Intron NP_000923.1
NM_001184883.1 1166 Intron NP_001171812.1
NM_001316314.1 1166 Intron NP_001303243.1
XM_011545101.2 1166 Intron XP_011543403.1
XM_017017925.1 1166 Intron XP_016873414.1

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