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AGCCAATGTGGGTGGTCAGCATCTG[A/C]AAACTGGACACCTTCTATTTCCCCT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610122 | |||||||||||||||||||||||
Literature Links: |
HTR3D 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 - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
HTR3D - 5-hydroxytryptamine receptor 3D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145143.1 | 473 | Missense Mutation | GAA,GCA | E,A 97 | NP_001138615.1 | |
NM_001163646.1 | 473 | Missense Mutation | GAA,GCA | E,A 158 | NP_001157118.1 | |
NM_182537.2 | 473 | Missense Mutation | GAA,GCA | E,A 23 | NP_872343.2 | |
XM_017005854.1 | 473 | Intron | XP_016861343.1 |