Product Details

SNP ID
rs144873026
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64270130 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGATCCTCTTTTTGCATAGGCCTGA[C/G]GGAAGTACTTCCGCCCATATTCAAG
Phenotype
MIM: 603167 MIM: 600230
Polymorphism
C/G, Transversion 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_004322.3 922 UTR 3 NP_004313.1
NM_032989.2 922 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_001170726.1 922 Intron NP_001164197.1
NM_001170880.1 922 Intron NP_001164351.1
NM_001170881.1 922 Intron NP_001164352.1
NM_001177358.1 922 Intron NP_001170829.1
NM_020155.3 922 Intron NP_064540.3
XM_005274100.2 922 Intron XP_005274157.1
XM_005274101.2 922 Intron XP_005274158.1
XM_005274102.2 922 Intron XP_005274159.1
XM_005274104.2 922 Intron XP_005274161.1
XM_011545168.2 922 Intron XP_011543470.1
XM_011545169.1 922 Intron XP_011543471.1
XM_011545170.2 922 Intron XP_011543472.1
XM_011545171.2 922 Intron XP_011543473.1
XM_011545172.2 922 Intron XP_011543474.1
XM_017018014.1 922 Intron XP_016873503.1
XM_017018015.1 922 Intron XP_016873504.1
XM_017018016.1 922 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_000932.2 922 Intron NP_000923.1
NM_001184883.1 922 Intron NP_001171812.1
NM_001316314.1 922 Intron NP_001303243.1
XM_011545101.2 922 Intron XP_011543403.1
XM_017017925.1 922 Intron XP_016873414.1

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