Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601122 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HTR2B 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)
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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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HTR2B - 5-hydroxytryptamine receptor 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000867.4 | 1716 | Missense Mutation | ATG,GTG | M,V 421 | NP_000858.3 | |
NM_001320758.1 | 1716 | Missense Mutation | ATG,GTG | M,V 379 | NP_001307687.1 | |
XM_005246520.3 | 1716 | Missense Mutation | ATG,GTG | M,V 302 | XP_005246577.1 | |
XM_006712482.2 | 1716 | Missense Mutation | ATG,GTG | M,V 396 | XP_006712545.1 |
PSMD1 - proteasome 26S subunit, non-ATPase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001191037.1 | 1716 | Intron | NP_001177966.1 | |||
NM_002807.3 | 1716 | Intron | NP_002798.2 | |||
XM_017004517.1 | 1716 | Intron | XP_016860006.1 |
Set Membership: |
HapMap |