chr1:19666020:C>T Detail (hg38) (HTR6)

Information

Genome

Assembly Position
hg19 chr1:19,992,513-19,992,513 View the variant detail on this assembly version.
hg38 chr1:19,666,020-19,666,020

HGVS

Type Transcript Protein
RefSeq NM_000871.2:c.267C>T NP_000862.1:p.Tyr89=
Ensemble ENST00000289753.2:c.267C>T ENST00000289753.2:p.Tyr89=
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:0.299
ToMMo:0.299
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:0.237

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601109 OMIM
HGNC 5301 HGNC
Ensembl ENSG00000158748 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv623842 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.011 Unipolar Depression In this study, we evaluated the association of seven serotonin signal transducti... BeFree 19590397 Detail
0.155 major depressive disorder In this study, we evaluated the association of seven serotonin signal transducti... BeFree 19590397 Detail
<0.001 dementia In order to identify gene variants related to the serotonergic neurotransmitter ... BeFree 11725820 Detail
<0.001 Presenile dementia In order to identify gene variants related to the serotonergic neurotransmitter ... BeFree 11725820 Detail
<0.001 Presenile dementia In order to identify gene variants related to the serotonergic neurotransmitter ... BeFree 11725820 Detail
<0.001 Unipolar Depression Association between the 5-HT6 receptor C267T polymorphism and response to antide... BeFree 15823158 Detail
<0.001 lingual-facial-buccal dyskinesia Genetic association analysis of 5-HT(6) receptor gene polymorphism (267C/T) with... BeFree 12057822 Detail
<0.001 Hallucinations In addition, the HTR6 T267C polymorphism has been linked to risperidone response... BeFree 15882132 Detail
<0.001 Tardive Dyskinesia Genetic association analysis of 5-HT(6) receptor gene polymorphism (267C/T) with... BeFree 12057822 Detail
<0.001 dementia In order to identify gene variants related to the serotonergic neurotransmitter ... BeFree 11725820 Detail
0.005 Mental Depression Association analysis of the 5-HT6 receptor polymorphism C267T with depression in... BeFree 11442897 Detail
0.003 major depressive disorder Association study of the 5-HT(6) receptor polymorphism (C267T) and symptomatolog... BeFree 11702016 Detail
<0.001 Delusions In addition, the HTR6 T267C polymorphism has been linked to risperidone response... BeFree 15882132 Detail
0.003 major depressive disorder Association between the 5-HT6 receptor C267T polymorphism and response to antide... BeFree 15823158 Detail
0.003 Mood Disorders Association analysis of the 5-HT(6) receptor polymorphism (C267T) in mood disord... BeFree 10581475 Detail
Annotation

Annotations

DescrptionSourceLinks
In this study, we evaluated the association of seven serotonin signal transduction-linked single nuc... DisGeNET Detail
In this study, we evaluated the association of seven serotonin signal transduction-linked single nuc... DisGeNET Detail
In order to identify gene variants related to the serotonergic neurotransmitter system that possibly... DisGeNET Detail
In order to identify gene variants related to the serotonergic neurotransmitter system that possibly... DisGeNET Detail
In order to identify gene variants related to the serotonergic neurotransmitter system that possibly... DisGeNET Detail
Association between the 5-HT6 receptor C267T polymorphism and response to antidepressant treatment i... DisGeNET Detail
Genetic association analysis of 5-HT(6) receptor gene polymorphism (267C/T) with tardive dyskinesia. DisGeNET Detail
In addition, the HTR6 T267C polymorphism has been linked to risperidone response for positive sympto... DisGeNET Detail
Genetic association analysis of 5-HT(6) receptor gene polymorphism (267C/T) with tardive dyskinesia. DisGeNET Detail
In order to identify gene variants related to the serotonergic neurotransmitter system that possibly... DisGeNET Detail
Association analysis of the 5-HT6 receptor polymorphism C267T with depression in patients with Alzhe... DisGeNET Detail
Association study of the 5-HT(6) receptor polymorphism (C267T) and symptomatology and antidepressant... DisGeNET Detail
In addition, the HTR6 T267C polymorphism has been linked to risperidone response for positive sympto... DisGeNET Detail
Association between the 5-HT6 receptor C267T polymorphism and response to antidepressant treatment i... DisGeNET Detail
Association analysis of the 5-HT(6) receptor polymorphism (C267T) in mood disorders. DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
Genome
hg38
Position
chr1:19,666,020-19,666,020
Variant Type
snv
Reference Allele
C
Alternative Allele
T
Filtering Status (HGVD)
PASS
# of samples (HGVD)
1209
Mean of sample read depth (HGVD)
214.52
Standard deviation of sample read depth (HGVD)
99.83
Number of reference allele (HGVD)
1694
Number of alternative allele (HGVD)
724
Allele Frequency (HGVD)
0.29942100909842845
Gene Symbol (HGVD)
HTR6
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs1805054
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.2993
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
5015
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16754
East Asian Chromosome Counts (ExAC)
8532
East Asian Allele Counts (ExAC)
2026
East Asian Heterozygous Counts (ExAC)
1504
East Asian Homozygous Counts (ExAC)
261
East Asian Allele Frequency (ExAC)
0.23745897796530707
Chromosome Counts in All Race (ExAC)
119954
Allele Counts in All Race (ExAC)
18136
Heterozygous Counts in All Race (ExAC)
15149
Homozygous Counts in All Race (ExAC)
1493
Allele Frequency in All Race (ExAC)
0.15119128999449788
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