Variant #0000280938 (NC_000016.9:g.31195715_31195720del, NC_000016.9(NM_004960.3):c.521_523+3del (FUS))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31195715_31195720del |
| DNA change (hg38) |
g.31184394_31184399del |
| Published as |
FUS(NM_004960.3):c.518_523delGTGGAG (p.G174_G175del), FUS(NM_004960.4):c.518_523delGTGGAG (p.G174_G175del), FUS(NM_004960.4):c.521_523+3delGAGGTG |
| ISCN |
- |
| DB-ID |
FUS_000125 See all 3 reported entries |
| 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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