Product Details

SNP ID
rs149903516
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:64270317 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCATCTGCGTTGCTGTGCCCGCGCT[C/T]TTCGGGCGAGGAAGTCCCTTCTGGT
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_004322.3 735 Silent Mutation AAA,AAG K133K NP_004313.1
NM_032989.2 735 Silent Mutation AAA,AAG K133K 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_001170726.1 735 Intron NP_001164197.1
NM_001170880.1 735 Intron NP_001164351.1
NM_001170881.1 735 Intron NP_001164352.1
NM_001177358.1 735 Intron NP_001170829.1
NM_020155.3 735 Intron NP_064540.3
XM_005274100.2 735 Intron XP_005274157.1
XM_005274101.2 735 Intron XP_005274158.1
XM_005274102.2 735 Intron XP_005274159.1
XM_005274104.2 735 Intron XP_005274161.1
XM_011545168.2 735 Intron XP_011543470.1
XM_011545169.1 735 Intron XP_011543471.1
XM_011545170.2 735 Intron XP_011543472.1
XM_011545171.2 735 Intron XP_011543473.1
XM_011545172.2 735 Intron XP_011543474.1
XM_017018014.1 735 Intron XP_016873503.1
XM_017018015.1 735 Intron XP_016873504.1
XM_017018016.1 735 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_000932.2 735 Intron NP_000923.1
NM_001184883.1 735 Intron NP_001171812.1
NM_001316314.1 735 Intron NP_001303243.1
XM_011545101.2 735 Intron XP_011543403.1
XM_017017925.1 735 Intron XP_016873414.1

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