chr4:186274193:G>T Detail (hg38) (F11)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr4:187,195,347-187,195,347 View the variant detail on this assembly version. |
| hg38 | chr4:186,274,193-186,274,193 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000128.3:c.403G>T | NP_000119.1:p.Glu135Ter |
| Ensemble | ENST00000403665.7:c.403G>T | ENST00000403665.7:p.Glu135Ter |
| ENST00000492972.6:c.403G>T | ENST00000492972.6:p.Glu135Ter |
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 |
Pathogenic
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
|
Pathogenic
|
2024-03-29 | criteria provided, multiple submitters, no conflicts | Hereditary factor XI deficiency disease |
germline
unknown
|
Detail |
|
Pathogenic
|
2024-02-06 | criteria provided, multiple submitters, no conflicts | not provided |
germline
|
Detail |
|
Pathogenic
|
2014-09-07 | criteria provided, single submitter | Inborn genetic diseases |
germline
|
Detail |
|
Pathogenic
|
2020-05-01 | no assertion criteria provided |
germline
|
Detail | |
|
Pathogenic
|
2020-09-16 | no assertion criteria provided | Plasma factor XI deficiency |
germline
|
Detail |
|
Pathogenic
|
2023-12-20 | criteria provided, single submitter | F11-related disorder |
germline
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.587 | factor XI deficiency | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND Hereditary factor XI deficiency disease | ClinVar | Detail |
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND not provided | ClinVar | Detail |
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND Inborn genetic diseases | ClinVar | Detail |
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND multiple conditions | ClinVar | Detail |
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND Plasma factor XI deficiency | ClinVar | Detail |
| NM_000128.4(F11):c.403G>T (p.Glu135Ter) AND F11-related disorder | ClinVar | Detail |
| NA | 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
- rs121965063 dbSNP
- Genome
- hg38
- Position
- chr4:186,274,193-186,274,193
- Variant Type
- snv
- Reference Allele
- G
- Alternative Allele
- T
- East Asian Chromosome Counts (ExAC)
- 8652
- 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)
- 121320
- Allele Counts in All Race (ExAC)
- 95
- Heterozygous Counts in All Race (ExAC)
- 93
- Homozygous Counts in All Race (ExAC)
- 1
- Allele Frequency in All Race (ExAC)
- 7.830530827563468E-4
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