chr22:30337586:T>C Detail (hg19) (MTMR3)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr22:30,337,586-30,337,586 |
| hg38 | chr22:29,941,597-29,941,597 View the variant detail on this assembly version. |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_153050.2:c.-137-15439T>C | |
| NM_153051.2:c.-137-15439T>C | ||
| NM_021090.3:c.-137-15439T>C |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:[No Data.] |
| ToMMo:0.928 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:[No Data.] |
Prediction
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.143 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.155 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.015 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.121 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.125 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| <0.001 | Malignant neoplasm of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.009 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.003 | Carcinoma of lung | The combined analyses identified six well-replicated SNPs with independent effec... | BeFree | 21725308 | Detail |
| 0.002 | Lung Neoplasms | [A genome-wide association study identifies two new lung cancer susceptibility l... | GAD | 21725308 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| The combined analyses identified six well-replicated SNPs with independent effects and significant l... | DisGeNET | Detail |
| [A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and ... | DisGeNET | Detail |
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- dbSNP
- rs36600 dbSNP
- Genome
- hg19
- Position
- chr22:30,337,586-30,337,586
- Variant Type
- snv
- Reference Allele
- T
- Alternative Allele
- C
- 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))
- rs36600
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.9283
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 15558
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
Genome browser