Variant #0001070241 (NC_000006.11:g.19066298_21763281inv)
| Individual ID |
00474045 |
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.19066298_21763281inv |
| DNA change (hg38) |
g.19066067_21763050inv |
| Published as |
g.19066067_21763050inv |
| ISCN |
- |
| DB-ID |
chr6_008321 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Elsa Lucas Castro |
| Database submission license |
No license selected |
| Created by |
Elsa Lucas Castro |
| Date created |
2026-03-09 10:33:37 +01:00 (CET) |
| Date last edited |
2026-03-30 15:22:51 +02:00 (CEST) |

Variant on transcripts
Screenings
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