Variant #0000457201 (NC_000002.11:g.(?_208091112)_(220083453_?)?)
| Individual ID |
00206608 |
| 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.(?_208091112)_(220083453_?)? |
| DNA change (hg38) |
g.(?_207226388)_(219218731_?)? |
| Published as |
- |
| ISCN |
2q33.3-q35 |
| DB-ID |
chr2_009511 |
| Variant remarks |
mapped to linkage region flanked by SNPs, rs717973 and rs1109867 |
| Reference |
Andres, under review 2019 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
razam |
| 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 |
2019-02-14 15:54:04 +01:00 (CET) |
| Date last edited |
2019-02-24 11:57:50 +01:00 (CET) |

Variant on transcripts
Screenings
|