Variant #0000566704 (NC_000019.9:g.19310062G>C, NM_001145783.1:c.-7136C>G (MEF2BNB))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.19310062G>C |
| DNA change (hg38) |
g.19199253G>C |
| Published as |
RFXANK(NM_003721.2):c.712+19G>C |
| ISCN |
- |
| DB-ID |
MEF2BNB_000001 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
1.0E-5 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|