Variant #0000061638 (NC_000002.11:g.(64084978_64107729)_(64565531_64568643)dup)
| Individual ID |
00034476 |
| Chromosome |
2 |
| Allele |
Paternal (confirmed) |
| 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.(64084978_64107729)_(64565531_64568643)dup |
| DNA change (hg38) |
- |
| Published as |
g.(64084978_64107729)_(64565531_64568643)dup |
| ISCN |
- |
| DB-ID |
chr2_000759 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marta Sanchez Castro |
| Database submission license |
No license selected |
| Created by |
Marta Sanchez Castro |
| Date created |
2015-03-19 15:37:25 +01:00 (CET) |
| Date last edited |
2015-05-05 15:14:27 +02:00 (CEST) |

Variant on transcripts
Screenings
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