chr16:3293310:A>T Detail (hg19) (MEFV)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr16:3,293,310-3,293,310 |
hg38 | chr16:3,243,310-3,243,310 View the variant detail on this assembly version. |
HGVS
Type | Transcript | Protein |
---|---|---|
RefSeq | NM_000243.2:c.2177T>A | NP_000234.1:p.Val726Asp |
NM_001198536.1:c.*381T>A | ||
Ensemble | ENST00000536379.5:c.1544T>A | ENST00000536379.5:p.Val515Asp |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
Frequency
JP | HGVD:[No Data.] |
ToMMo:[No Data.] | |
NCBN:[No Data.] | |
NCBN(Hondo):[No Data.] | |
NCBN(Ryukyu):[No Data.] | |
East asia | ExAC:<0.001 |
Prediction
ClinVar
Clinical Significance |
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Review star | ![]() |
Show details |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
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2023-10-11 | criteria provided, single submitter | not specified |
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Detail |
CIViC
[No Data.]
DisGeNET
Score | Disease name | Description | Source | Pubmed | Links |
---|---|---|---|---|---|
0.753 | familial Mediterranean fever | We screened 207 BD patients who had no symptoms and family history for FMF and 2... | BeFree | 23973724 | Detail |
0.753 | familial Mediterranean fever | NA | CLINVAR | Detail | |
0.753 | familial Mediterranean fever | Pyrin/marenostrin mutations in familial Mediterranean fever. | UNIPROT | 10024914 | Detail |
<0.001 | Coronary heart disease | To evaluate whether inflammatory alleles of pyrin, the gene responsible for fami... | BeFree | 16387839 | Detail |
0.753 | familial Mediterranean fever | To evaluate whether inflammatory alleles of pyrin, the gene responsible for fami... | BeFree | 16387839 | Detail |
0.010 | Henoch-Schoenlein purpura | MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with He... | BeFree | 22783597 | Detail |
0.753 | familial Mediterranean fever | The MEFV gene involved in familial Mediterranean fever was recently cloned and f... | BeFree | 10447272 | Detail |
0.753 | familial Mediterranean fever | The aim of this study is to evaluate the use of polymerase chain reaction (PCR) ... | BeFree | 15724392 | Detail |
0.064 | amyloidosis | We compared the frequencies of seven MEFV mutations (M694V, M680I, V726A, M694I,... | BeFree | 11029479 | Detail |
0.753 | familial Mediterranean fever | Eight MEFV gene variants (M694I, M694V, M680I (G/C-A), V726A, R761H, E148Q and P... | BeFree | 22351163 | Detail |
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
NM_000243.3(MEFV):c.2177T>A (p.Val726Asp) AND not specified | ClinVar | Detail |
We screened 207 BD patients who had no symptoms and family history for FMF and 200 healthy subjects ... | DisGeNET | Detail |
NA | DisGeNET | Detail |
Pyrin/marenostrin mutations in familial Mediterranean fever. | DisGeNET | Detail |
To evaluate whether inflammatory alleles of pyrin, the gene responsible for familial Mediterranean f... | DisGeNET | Detail |
To evaluate whether inflammatory alleles of pyrin, the gene responsible for familial Mediterranean f... | DisGeNET | Detail |
MEFV gene mutations (M694V, V726A, M680I, and A744S) in Iranian children with Henoch-Schönlein purpu... | DisGeNET | Detail |
The MEFV gene involved in familial Mediterranean fever was recently cloned and four distinct sequenc... | DisGeNET | Detail |
The aim of this study is to evaluate the use of polymerase chain reaction (PCR) for diagnosis of FMF... | DisGeNET | Detail |
We compared the frequencies of seven MEFV mutations (M694V, M680I, V726A, M694I, K695R, R761H, E148Q... | DisGeNET | Detail |
Eight MEFV gene variants (M694I, M694V, M680I (G/C-A), V726A, R761H, E148Q and P369S) were analyzed ... | 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
- -
- Genome
- hg19
- Position
- chr16:3,293,310-3,293,310
- Variant Type
- snv
- Reference Allele
- A
- Alternative Allele
- T
- East Asian Chromosome Counts (ExAC)
- 8654
- East Asian Allele Counts (ExAC)
- 0
- East Asian Heterozygous Counts (ExAC)
- 0
- East Asian Homozygous Counts (ExAC)
- 0
- East Asian Allele Frequency (ExAC)
- 0.0
- Chromosome Counts in All Race (ExAC)
- 121408
- Allele Counts in All Race (ExAC)
- 1
- Heterozygous Counts in All Race (ExAC)
- 1
- Homozygous Counts in All Race (ExAC)
- 0
- Allele Frequency in All Race (ExAC)
- 8.236689509752241E-6
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