Variant #0001020920 (NC_000016.9:g.pter_3970809delins[NC_000017.10:g.pter_1277413])
| Individual ID |
00459554 |
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.pter_3970809delins[NC_000017.10:g.pter_1277413] |
| DNA change (hg38) |
g.pter_3920808delins[NC_000017.11:g.pter_1374119] |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr16_006858 |
| Variant remarks |
- |
| Reference |
- |
| 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 |
Rikke Christensen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-01-14 18:17:37 +01:00 (CET) |
| Date last edited |
2025-01-14 18:17:59 +01:00 (CET) |
Variant on transcripts
Screenings
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