Variant #0000169155 (NC_000011.9:g.2021134_2021176|gom)
| Individual ID |
00103960 |
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2021134_2021176|gom |
| DNA change (hg38) |
g.1999904_1999946|gom |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr11_000773 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Somatic |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
0.83 |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Jack Brzezinski |
| Database submission license |
No license selected |
| Created by |
Jack Brzezinski |
| Date created |
2017-04-26 15:42:25 +02:00 (CEST) |
| Date last edited |
2019-07-31 12:46:16 +02:00 (CEST) |

Variant on transcripts
Screenings
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