Product Details

SNP ID

rs199759687

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:64270228 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGAAGGTCACTGGGAGGGGGCGGAG[C/G]TTCCCCTGCCCAAGTTCCGATCCCA

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	824	Missense Mutation	ACC,AGC	T163S	NP_004313.1
NM_032989.2	824	Missense Mutation	ACC,AGC	T163S	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	824	Intron			NP_001164197.1
NM_001170880.1	824	Intron			NP_001164351.1
NM_001170881.1	824	Intron			NP_001164352.1
NM_001177358.1	824	Intron			NP_001170829.1
NM_020155.3	824	Intron			NP_064540.3
XM_005274100.2	824	Intron			XP_005274157.1
XM_005274101.2	824	Intron			XP_005274158.1
XM_005274102.2	824	Intron			XP_005274159.1
XM_005274104.2	824	Intron			XP_005274161.1
XM_011545168.2	824	Intron			XP_011543470.1
XM_011545169.1	824	Intron			XP_011543471.1
XM_011545170.2	824	Intron			XP_011543472.1
XM_011545171.2	824	Intron			XP_011543473.1
XM_011545172.2	824	Intron			XP_011543474.1
XM_017018014.1	824	Intron			XP_016873503.1
XM_017018015.1	824	Intron			XP_016873504.1
XM_017018016.1	824	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	824	Intron			NP_000923.1
NM_001184883.1	824	Intron			NP_001171812.1
NM_001316314.1	824	Intron			NP_001303243.1
XM_011545101.2	824	Intron			XP_011543403.1
XM_017017925.1	824	Intron			XP_016873414.1

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