chr19:41858876:C>G Detail (hg19) (TGFB1, TMEM91)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr19:41,858,876-41,858,876 |
hg38 | chr19:41,352,971-41,352,971 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000660.5:c.74G>C | NP_000651.3:p.Arg25Pro |
Ensemble | ENST00000221930.6:c.74G>C | ENST00000221930.6:p.Arg25Pro |
ENST00000600196.2:c.74G>C | ENST00000600196.2:p.Arg25Pro |
Type | Transcript | Protein |
---|---|---|
RefSeq | ||
Ensemble | ENST00000539627.5:c.-30+1769C>G |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:<0.001 |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:0.003 |
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.005 | Hepatitis C, Chronic | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.002 | Fibrosis, Liver | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.005 | Hepatitis C, Chronic | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.002 | Fibrosis, Liver | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.036 | Hepatitis C, Chronic | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.001 | Virus Diseases | The aim of this work was to establish an association between the single-nucleoti... | BeFree | 23941979 | Detail |
0.010 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
0.127 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
0.001 | schizophrenia | This study aimed at investigating the association between schizophrenia suscepti... | BeFree | 24065520 | Detail |
0.027 | Malignant neoplasm of prostate | We evaluated the influence of the TGFB1 polymorphisms by ARMS-PCR, Leu10Pro, and... | BeFree | 18058470 | Detail |
0.001 | Moyamoya disease | As no new genetic variants were uncovered in this study of the first exon of TGF... | BeFree | 22659181 | Detail |
0.009 | prostate carcinoma | We evaluated the influence of the TGFB1 polymorphisms by ARMS-PCR, Leu10Pro, and... | BeFree | 18058470 | Detail |
<0.001 | Moyamoya disease 1 | As no new genetic variants were uncovered in this study of the first exon of TGF... | BeFree | 22659181 | Detail |
0.001 | Chronic Kidney Diseases | The rs1800471 Polymorphism of TGFB1 Gene, Serum TGF-Beta1 Level and Chronic Kidn... | BeFree | 25298263 | Detail |
<0.001 | Chronic interstitial nephritis | In conclusion, rs1800471 polymorphism in TGFB1 gene does not have an impact on t... | BeFree | 25298263 | Detail |
0.005 | Graves Disease | Arg25Pro (c.915G>C) polymorphism of transforming growth factor β1 gene increa... | BeFree | 24742542 | Detail |
0.024 | rheumatoid arthritis | The functional class evaluated in rheumatoid arthritis is associated with solubl... | BeFree | 21113716 | Detail |
<0.001 | Chronic Kidney Insufficiency | The rs1800471 Polymorphism of TGFB1 Gene, Serum TGF-Beta1 Level and Chronic Kidn... | BeFree | 25298263 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000660.7(TGFB1):c.74G>C (p.Arg25Pro) AND not specified | ClinVar | Detail |
NM_000660.7(TGFB1):c.74G>C (p.Arg25Pro) AND not provided | ClinVar | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
The aim of this work was to establish an association between the single-nucleotide polymorphisms (SN... | DisGeNET | Detail |
This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
This study aimed at investigating the association between schizophrenia susceptibility and selected ... | DisGeNET | Detail |
We evaluated the influence of the TGFB1 polymorphisms by ARMS-PCR, Leu10Pro, and Arg25Pro, on prosta... | DisGeNET | Detail |
As no new genetic variants were uncovered in this study of the first exon of TGFB1 in European MMD p... | DisGeNET | Detail |
We evaluated the influence of the TGFB1 polymorphisms by ARMS-PCR, Leu10Pro, and Arg25Pro, on prosta... | DisGeNET | Detail |
As no new genetic variants were uncovered in this study of the first exon of TGFB1 in European MMD p... | DisGeNET | Detail |
The rs1800471 Polymorphism of TGFB1 Gene, Serum TGF-Beta1 Level and Chronic Kidney Disease Progressi... | DisGeNET | Detail |
In conclusion, rs1800471 polymorphism in TGFB1 gene does not have an impact on the development and p... | DisGeNET | Detail |
Arg25Pro (c.915G>C) polymorphism of transforming growth factor β1 gene increases the risk of deve... | DisGeNET | Detail |
The functional class evaluated in rheumatoid arthritis is associated with soluble TGF-β1 serum level... | DisGeNET | Detail |
The rs1800471 Polymorphism of TGFB1 Gene, Serum TGF-Beta1 Level and Chronic Kidney Disease Progressi... | 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
- rs1800471 dbSNP
- Genome
- hg19
- Position
- chr19:41,858,876-41,858,876
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- G
- Filtering Status (HGVD)
- PASS
- Filtering Status (HGVD)
- LowQual
- # of samples (HGVD)
- 1006
- Mean of sample read depth (HGVD)
- 26.38
- Standard deviation of sample read depth (HGVD)
- 13.20
- Number of reference allele (HGVD)
- 2011
- Number of alternative allele (HGVD)
- 1
- Allele Frequency (HGVD)
- 4.970178926441351E-4
- Gene Symbol (HGVD)
- TGFB1
- East Asian Chromosome Counts (ExAC)
- 368
- East Asian Allele Counts (ExAC)
- 1
- East Asian Heterozygous Counts (ExAC)
- 1
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.002717391304347826
- Chromosome Counts in All Race (ExAC)
- 15146
- Allele Counts in All Race (ExAC)
- 1200
- Heterozygous Counts in All Race (ExAC)
- 1120
- Homozygous Counts in All Race (ExAC)
- 40
- Allele Frequency in All Race (ExAC)
- 0.0792288392975043
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