Variant #0000276625 (NC_000003.11:g.10088410_10088413del, NC_000003.11(NM_001018115.1):c.1278+3_1278+6del (FANCD2))
| Chromosome |
3 |
| Allele |
Unknown |
| 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.10088410_10088413del |
| DNA change (hg38) |
g.10046726_10046729del |
| Published as |
FANCD2(NM_001319984.1):c.1278_1278+3delAGTA, FANCD2(NM_033084.3):c.1278_1278+3delAGTA |
| ISCN |
- |
| DB-ID |
FANCD2_000059 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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