All variants in the HTR3A gene

University of Heidelberg Serotonin receptor variant database
Information The variants shown are described using the NM_000869.5 transcript reference sequence.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/-? 3i c.282+7A>C r.(?) p.(=) - - likely benign g.113850006A>C g.113979284A>C IVS3+7A>C - HTR3A_000010 - PubMed: Niesler 2001b - rs61905785 Germline - 6/96 (6.25%) +CviKI_1 0 - Louise Amlie-Wolf
-?/-? 3i c.282+7A>C r.(?) p.(=) - - likely benign g.113850006A>C g.113979284A>C IVS3+7A>C - HTR3A_000010 - PubMed: Niesler 2001b - - Germline - 5/96 (5.2%) +CviKI_1 0 - Louise Amlie-Wolf
-?/? 3i c.282+7A>C r.(?) p.(=) - - likely benign g.113850006A>C g.113979284A>C IVS3+7A>C - HTR3A_000010 - PubMed: Frank 2004 - - Germline - 8/96 FM (5/96 Controls) +CviKI_1 0 - Louise Amlie-Wolf
-?/-? 3i c.282+7A>C r.(?) p.(=) - - likely benign g.113850006A>C g.113979284A>C IVS3+7A>C - HTR3A_000010 - PubMed: Niesler 2005 - - Germline - 8/47 GTS; 5/48 Controls +CviKI_1 0 - Louise Amlie-Wolf
-?/-? 3i c.282+7A>C r.(?) p.(=) - - likely benign g.113850006A>C g.113979284A>C IVS3+7A>C - HTR3A_000010 - PubMed: Niesler 2001b - - Germline - 9/140 (6.4 %) +CviKI_1 0 - Louise Amlie-Wolf
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