Variant #0000959675 (NC_000011.9:g.pter_35077342delins[NC_000012.11:g.pter_23711182])
| Individual ID |
00447894 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.pter_35077342delins[NC_000012.11:g.pter_23711182] |
| DNA change (hg38) |
g.pter_35055795delins[NC_000012.12:g.pter_23558248 |
| Published as |
- |
| ISCN |
46,XX,t(11;12)(p13;p12.1)dn |
| DB-ID |
chr11_008017 |
| Variant remarks |
- |
| Reference |
PubMed: Lamb 2012 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-01-31 17:58:05 +01:00 (CET) |
| Date last edited |
2024-01-31 18:00:29 +01:00 (CET) |
Variant on transcripts
Screenings
|