Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603167 MIM: 600230 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BAD PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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BAD - BCL2 associated agonist of cell death | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004322.3 | 1117 | UTR 3 | NP_004313.1 | |||
NM_032989.2 | 1117 | UTR 3 | NP_116784.1 |
GPR137 - G protein-coupled receptor 137 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170726.1 | 1117 | Intron | NP_001164197.1 | |||
NM_001170880.1 | 1117 | Intron | NP_001164351.1 | |||
NM_001170881.1 | 1117 | Intron | NP_001164352.1 | |||
NM_001177358.1 | 1117 | Intron | NP_001170829.1 | |||
NM_020155.3 | 1117 | Intron | NP_064540.3 | |||
XM_005274100.2 | 1117 | Intron | XP_005274157.1 | |||
XM_005274101.2 | 1117 | Intron | XP_005274158.1 | |||
XM_005274102.2 | 1117 | Intron | XP_005274159.1 | |||
XM_005274104.2 | 1117 | Intron | XP_005274161.1 | |||
XM_011545168.2 | 1117 | Intron | XP_011543470.1 | |||
XM_011545169.1 | 1117 | Intron | XP_011543471.1 | |||
XM_011545170.2 | 1117 | Intron | XP_011543472.1 | |||
XM_011545171.2 | 1117 | Intron | XP_011543473.1 | |||
XM_011545172.2 | 1117 | Intron | XP_011543474.1 | |||
XM_017018014.1 | 1117 | Intron | XP_016873503.1 | |||
XM_017018015.1 | 1117 | Intron | XP_016873504.1 | |||
XM_017018016.1 | 1117 | Intron | XP_016873505.1 |
PLCB3 - phospholipase C beta 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000932.2 | 1117 | Intron | NP_000923.1 | |||
NM_001184883.1 | 1117 | Intron | NP_001171812.1 | |||
NM_001316314.1 | 1117 | Intron | NP_001303243.1 | |||
XM_011545101.2 | 1117 | Intron | XP_011543403.1 | |||
XM_017017925.1 | 1117 | Intron | XP_016873414.1 |