chr11:5225714:C>T Detail (hg38) (HBB, LOC107133510, LOC110006319)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr11:5,246,944-5,246,944 View the variant detail on this assembly version. |
| hg38 | chr11:5,225,714-5,225,714 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
| RefSeq | NM_000518.4:c.328G>A | NP_000509.1:p.Val110Met |
| Ensemble | ENST00000335295.4:c.328G>A | ENST00000335295.4:p.Val110Met |
| ENST00000647020.1:c.328G>A | ENST00000647020.1:p.Val110Met |
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
ClinVar
| Clinical Significance |
Pathogenic
Likely pathogenic
|
| Review star |  |
| Show details | |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
| Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
|---|---|---|---|---|---|
other
|
2017-12-12 | no assertion criteria provided |
germline
|
Detail | |
|
Likely pathogenic
|
2015-02-17 | criteria provided, single submitter | beta thalassemia |
unknown
|
Detail |
|
Pathogenic
|
1995-01-01 | no assertion criteria provided | Erythrocytosis, familial, 6 |
germline
|
Detail |
|
Pathogenic
|
2021-07-16 | criteria provided, single submitter | hemoglobinopathy |
germline
|
Detail |
|
Pathogenic
|
2023-03-06 | criteria provided, multiple submitters, no conflicts | not provided |
germline
unknown
|
Detail |
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| 0.672 | beta thalassemia | NA | CLINVAR | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NM_000518.5(HBB):c.328G>A (p.Val110Met) AND HEMOGLOBIN SAN DIEGO | ClinVar | Detail |
| NM_000518.5(HBB):c.328G>A (p.Val110Met) AND beta Thalassemia | ClinVar | Detail |
| NM_000518.5(HBB):c.328G>A (p.Val110Met) AND Erythrocytosis, familial, 6 | ClinVar | Detail |
| NM_000518.5(HBB):c.328G>A (p.Val110Met) AND Hemoglobinopathy | ClinVar | Detail |
| NM_000518.5(HBB):c.328G>A (p.Val110Met) AND not provided | 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
- rs33969677 dbSNP
- Genome
- hg38
- Position
- chr11:5,225,714-5,225,714
- Variant Type
- snv
- Reference Allele
- C
- Alternative Allele
- T
Genome browser