Variant #0000571557 (NC_000022.10:g.24143269G>A, NC_000022.10(NM_003073.3):c.500+1G>A (SMARCB1))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.24143269G>A |
| DNA change (hg38) |
g.23801082G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SMARCB1_000113 See all 9 reported entries |
| 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) |
Retrieve |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-17 11:34:41 +02:00 (CEST) |

Variant on transcripts
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