Variant #0001010082 (NC_000005.9:g.7883859T>C, NC_000005.9(NM_002454.2):c.903+469T>C (MTRR))
| Chromosome |
5 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7883859T>C |
| DNA change (hg38) |
g.7883746T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MTRR_000069 See all 8 reported entries |
| Variant remarks |
expression cloning beta globin mini-gene splicing construct; variant suggested to create a new exonic splicing enhancer (ESE) |
| Reference |
PubMed: Homolova 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-09-27 16:11:54 +02:00 (CEST) |
| Date last edited |
2024-09-27 18:50:10 +02:00 (CEST) |

Variant on transcripts
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