chr10:99804058:G>A Detail (hg38) (ABCC2)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr10:101,563,815-101,563,815 View the variant detail on this assembly version. |
| hg38 | chr10:99,804,058-99,804,058 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | ||
| Ensemble | ENST00000647814.1:c.1249G>A | ENST00000647814.1:p.Val417Ile |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
| JP | HGVD:0.113 |
| ToMMo:0.129 | |
| NCBN:[No Data.] | |
| NCBN(Hondo):[No Data.] | |
| NCBN(Ryukyu):[No Data.] | |
| East asia | ExAC:0.085 |
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 |
|---|---|---|---|---|---|
|
|
2018-05-08 | criteria provided, multiple submitters, no conflicts | not specified |
|
Detail |
|
|
2021-07-14 | criteria provided, multiple submitters, no conflicts | Dubin-Johnson syndrome |
|
Detail |
|
|
2024-02-01 | criteria provided, multiple submitters, no conflicts | not provided |
|
Detail |
|
|
2023-01-16 | criteria provided, single submitter | ABCC2-related disorder |
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | Adenocarcinoma of large intestine | In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2... | BeFree | 16107775 | Detail |
| 0.001 | Adenocarcinoma of large intestine | In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2... | BeFree | 16107775 | Detail |
| <0.001 | Adenocarcinoma of large intestine | In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2... | BeFree | 16107775 | Detail |
| <0.001 | Adenocarcinoma of large intestine | In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2... | BeFree | 16107775 | Detail |
| <0.001 | Clear-cell metastatic renal cell carcinoma | The DNA of all patients was genotyped for ABCB1 -2352G>A, -692T>C, 2677G&g... | BeFree | 16788565 | Detail |
| <0.001 | Clear-cell metastatic renal cell carcinoma | The DNA of all patients was genotyped for ABCB1 -2352G>A, -692T>C, 2677G&g... | BeFree | 16788565 | Detail |
| 0.008 | colorectal cancer | The correlation of G1249A ABCC2 polymorphism with the development of colorectal ... | BeFree | 23232902 | Detail |
| 0.001 | colorectal carcinoma | The correlation of G1249A ABCC2 polymorphism with the development of colorectal ... | BeFree | 23232902 | Detail |
| 0.009 | epilepsy | The recessive model of MRP2 G1249A polymorphism decrease the risk of drug-resist... | BeFree | 25847339 | Detail |
| 0.009 | epilepsy | ABCC2 rs2273697 and rs3740066 polymorphisms and resistance to antiepileptic drug... | BeFree | 24624913 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) AND not specified | ClinVar | Detail |
| NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) AND Dubin-Johnson syndrome | ClinVar | Detail |
| NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) AND not provided | ClinVar | Detail |
| NM_000392.5(ABCC2):c.1249G>A (p.Val417Ile) AND ABCC2-related disorder | ClinVar | Detail |
| In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2 were additionally e... | DisGeNET | Detail |
| In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2 were additionally e... | DisGeNET | Detail |
| In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2 were additionally e... | DisGeNET | Detail |
| In this study, 3 genotypes of MDR1, 4 genotypes of MRP1, and 6 genotypes of MRP2 were additionally e... | DisGeNET | Detail |
| The DNA of all patients was genotyped for ABCB1 -2352G>A, -692T>C, 2677G>T/A (Ala893Ser/Thr... | DisGeNET | Detail |
| The DNA of all patients was genotyped for ABCB1 -2352G>A, -692T>C, 2677G>T/A (Ala893Ser/Thr... | DisGeNET | Detail |
| The correlation of G1249A ABCC2 polymorphism with the development of colorectal cancer (CRC) and poo... | DisGeNET | Detail |
| The correlation of G1249A ABCC2 polymorphism with the development of colorectal cancer (CRC) and poo... | DisGeNET | Detail |
| The recessive model of MRP2 G1249A polymorphism decrease the risk of drug-resistant in Asian Epileps... | DisGeNET | Detail |
| ABCC2 rs2273697 and rs3740066 polymorphisms and resistance to antiepileptic drugs in Asia Pacific ep... | 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
- rs2273697 dbSNP
- Genome
- hg38
- Position
- chr10:99,804,058-99,804,058
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- A
- Filtering Status (HGVD)
- PASS
- # of samples (HGVD)
- 1208
- Mean of sample read depth (HGVD)
- 52.36
- Standard deviation of sample read depth (HGVD)
- 22.69
- Number of reference allele (HGVD)
- 2142
- Number of alternative allele (HGVD)
- 274
- Allele Frequency (HGVD)
- 0.11341059602649006
- Gene Symbol (HGVD)
- ABCC2
- 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))
- rs2273697
- Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 0.1288
- Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 2159
- Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
- 16760
- East Asian Chromosome Counts (ExAC)
- 8638
- East Asian Allele Counts (ExAC)
- 735
- East Asian Heterozygous Counts (ExAC)
- 659
- East Asian Homozygous Counts (ExAC)
- 38
- East Asian Allele Frequency (ExAC)
- 0.08508914100486224
- Chromosome Counts in All Race (ExAC)
- 121328
- Allele Counts in All Race (ExAC)
- 23695
- Heterozygous Counts in All Race (ExAC)
- 18771
- Homozygous Counts in All Race (ExAC)
- 2462
- Allele Frequency in All Race (ExAC)
- 0.19529704602400105
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