Variant #0000017971 (NC_000002.11:g.75897433_75897467del, NC_000002.11(NM_003203.4):c.1957-57_1957-23del (GCFC2))
| Chromosome |
2 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75897433_75897467del |
| DNA change (hg38) |
g.75670307_75670341del |
| Published as |
delTATGTACCTTTTCTCCAAAGAGAAACTGTAATAGT |
| ISCN |
- |
| DB-ID |
GCFC2_000002 |
| Variant remarks |
variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
1 |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-05-06 10:00:16 +02:00 (CEST) |
| Date last edited |
2025-03-11 13:26:07 +01:00 (CET) |

Variant on transcripts
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