Variant #0000460209 (NC_000002.11:g.(?_111705738)_(133160621_?)?)
| Individual ID |
00224974 |
| Chromosome |
2 |
| Allele |
Both (homozygous) |
| 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.(?_111705738)_(133160621_?)? |
| DNA change (hg38) |
g.(?_110948161_(132403048_?)? |
| Published as |
- |
| ISCN |
2q13-q21.2 |
| DB-ID |
chr2_009514 |
| Variant remarks |
mapped to homozygous region flanked by SNPs rs729386 to rs2872920 |
| Reference |
Andres, under review 2019 |
| 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 |
Johan den Dunnen |
| Date created |
2019-02-24 13:50:40 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
|