Variant #0000595090 (NC_000015.9:g.(?_77926103)_(86940622_?)?)
| Individual ID |
00263418 |
| Chromosome |
15 |
| Allele |
Parent #1 |
| 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.(?_77926103)_(86940622_?)? |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
15q24.3-q25.3 |
| DB-ID |
chr15_004899 |
| Variant remarks |
Mapped to the linkage region flanked by SNPs rs74025333 and rs4362360 |
| Reference |
Andres, 2019 under review |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
M. Hashim Raza |
| Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
| Created by |
M. Hashim Raza |
| Date created |
2019-08-28 23:35:08 +02:00 (CEST) |
| Date last edited |
2019-08-30 11:46:12 +02:00 (CEST) |

Variant on transcripts
Screenings
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