Variant #0000874847 (NC_000022.10:g.?, NM_000631.4:c.? (NCF4))
| Chromosome |
22 |
| 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.? |
| DNA change (hg38) |
- |
| Published as |
815C>T (P272L), 815G>A (P272L) |
| ISCN |
- |
| DB-ID |
NCF4_000000 |
| Variant remarks |
- |
| Reference |
PubMed: Roos 2021, Journal: Roos 2021, PubMed: Lee 2006, Journal: Lee 2006 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-08-13 08:55:00 +02:00 (CEST) |
| Date last edited |
2022-08-13 08:55:49 +02:00 (CEST) |
Variant on transcripts
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