Variant #0000442535 (NC_000019.9:g.(?_6904195)_(7103542_?)dup)
| Individual ID |
00210051 |
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_6904195)_(7103542_?)dup |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr19_003340 |
| Variant remarks |
- |
| Reference |
PubMed: Vadgama 2019, Journal: Vadgama 2019 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Nirmal Vadgama |
| Database submission license |
No license selected |
| Created by |
Nirmal Vadgama |
| Date created |
2018-12-26 03:25:24 +01:00 (CET) |
| Date last edited |
2019-07-02 07:59:54 +02:00 (CEST) |

Variant on transcripts
Screenings
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