chr7:99367825:T>A Detail (hg19) (CYP3A4)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr7:99,367,825-99,367,825 |
hg38 | chr7:99,770,202-99,770,202 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_001202855.2:c.352A>T | NP_001189784.1:p.Ile118Phe |
NM_017460.5:c.352A>T | NP_059488.2:p.Ile118Phe | |
Ensemble | ENST00000336411.7:c.352A>T | ENST00000336411.7:p.Ile118Phe |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.130 | Hypercholesterolemia | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.008 | Hypercholesterolemia | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.006 | Hypertensive disease | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.018 | Hypertensive disease | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.428 | Hypercholesterolemia | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.005 | Hypertensive disease | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.008 | Hypertensive disease | Evaluation of genotype distributions by the Chi-square test and subsequent multi... | BeFree | 18097620 | Detail |
0.003 | Cerebrovascular accident | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
0.003 | Cerebrovascular accident | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | Subarachnoid Hemorrhage | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
0.006 | cerebral infarction | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
0.011 | Cerebrovascular accident | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | cerebral infarction | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | Subarachnoid Hemorrhage | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | cerebral infarction | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | cerebral infarction | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
<0.001 | Cerebrovascular accident | An initial chi(2) test (false discovery rate <0.05) and subsequent multivaria... | BeFree | 18566305 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
Evaluation of genotype distributions by the Chi-square test and subsequent multivariable logistic re... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | DisGeNET | Detail |
An initial chi(2) test (false discovery rate <0.05) and subsequent multivariable logistic-regress... | 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
- -
- dbSNP
- rs55951658 dbSNP
- Genome
- hg19
- Position
- chr7:99,367,825-99,367,825
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- A
Genome browser