chr16:55477894:C>T Detail (hg38) (MMP2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr16:55,511,806-55,511,806 View the variant detail on this assembly version. |
| hg38 | chr16:55,477,894-55,477,894 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | ||
| Ensemble | ENST00000570308.5:c.-75-5015C>T |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.069 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance |
|
| Review star | ![]() |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
|
2016-01-01 | criteria provided, single submitter | Lip and oral cavity carcinoma |
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | Glaucoma, Open-Angle | Functional gene polymorphisms of these MMPs such as MMP1 -1607 1G/2G (rs1799750)... | BeFree | 20808730 | Detail |
| 0.006 | Malignant neoplasm of urinary bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| <0.001 | Carcinoma of bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| <0.001 | Malignant neoplasm of urinary bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| <0.001 | Carcinoma of bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| <0.001 | Malignant neoplasm of urinary bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| <0.001 | Carcinoma of bladder | To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 ... | BeFree | 23819551 | Detail |
| 0.133 | rheumatoid arthritis | The MMP2 rs243865-T allele is not a major genetic factor for rheumatoid arthriti... | BeFree | 18205826 | Detail |
| 0.008 | Malignant neoplasm of urinary bladder | The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs39... | BeFree | 23819551 | Detail |
| 0.004 | Carcinoma of bladder | The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs39... | BeFree | 23819551 | Detail |
| 0.005 | Carcinoma of bladder | The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs39... | BeFree | 23819551 | Detail |
| 0.012 | Malignant neoplasm of urinary bladder | The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs39... | BeFree | 23819551 | Detail |
| 0.005 | Secondary malignant neoplasm of lymph node | Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of... | BeFree | 21612407 | Detail |
| 0.009 | stomach carcinoma | Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of... | BeFree | 21612407 | Detail |
| 0.013 | Malignant neoplasm of stomach | Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of... | BeFree | 21612407 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_004530.5(MMP2):c.-1586C>T AND Lip and oral cavity carcinoma | ClinVar | Detail |
| Functional gene polymorphisms of these MMPs such as MMP1 -1607 1G/2G (rs1799750), MMP2 -1306 C/T (rs... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| To elucidate genetic polymorphisms of the matrix metalloproteinases (MMPs) MMP1 (rs1799750), MMP2 (r... | DisGeNET | Detail |
| The MMP2 rs243865-T allele is not a major genetic factor for rheumatoid arthritis in the French Cauc... | DisGeNET | Detail |
| The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs3918242) allele T was ... | DisGeNET | Detail |
| The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs3918242) allele T was ... | DisGeNET | Detail |
| The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs3918242) allele T was ... | DisGeNET | Detail |
| The combined genotype MMP2 -1306C/T (rs243865) allele T with MMP9 -1562C/T (rs3918242) allele T was ... | DisGeNET | Detail |
| Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of GC. | DisGeNET | Detail |
| Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of GC. | DisGeNET | Detail |
| Epistasis between PARP1 rs1136410 and MMP2 rs243865 increased the risk of LNM of GC. | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs243865 dbSNP
- Genome
- hg38
- Position
- chr16:55,477,894-55,477,894
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
- 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))
- rs243865
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.0693
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 1161
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
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