Variant #0000116113 (NC_000001.10:g.(?_241660857)_(241683085_?)del, FH(NM_000143.3):c.(?_-63)_(*271_?)del)
Individual ID |
00072978 |
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_241660857)_(241683085_?)del |
DNA change (hg38) |
- |
Published as |
c.1-? c.*100del |
ISCN |
- |
DB-ID |
FH_000001 See all 6 reported entries |
Variant remarks |
whole-gene deletion |
Reference |
PubMed: Smit |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
Jean-Pierre Bayley |
Database submission license |
Creative Commons Attribution-NonCommercial 4.0 International |
Created by |
Jean-Pierre Bayley |

Variant on transcripts
Screenings
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