Variant #0000557958 (NC_000016.9:g.31195715_31195720dup, NC_000016.9(NM_004960.3):c.521_523+3dup (FUS))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.31195715_31195720dup |
DNA change (hg38) |
g.31184394_31184399dup |
Published as |
FUS(NM_004960.3):c.520_525dupGGAGGT (p.G174_G175dup) |
ISCN |
- |
DB-ID |
FUS_000182 |
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 |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-07-09 15:51:41 +02:00 (CEST) |

Variant on transcripts
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