Variant #0000665606 (NC_000017.10:[NC_000001.10:g.(185800001_198700000)_qter]delins(70900001_qter))
| Individual ID |
00080105 |
| Chromosome |
17 |
| 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) |
[NC_000001.10:g.(185800001_198700000)_qter]delins(70900001_qter) |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr17_007857 |
| Variant remarks |
- |
| Reference |
for EUCID-SRS consortium |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
DUPLICATE record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-05-10 14:42:46 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:54:17 +02:00 (CEST) |
Variant on transcripts
Screenings
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