Variant #0001015375 (NC_000016.9:g.2506800G>A, NM_025108.2:c.-3346G>A (C16orf59))
| 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.2506800G>A |
| DNA change (hg38) |
- |
| Published as |
CCNF(NM_001761.3):c.2140G>A (p.V714M) |
| ISCN |
- |
| DB-ID |
CCNF_000004 |
| 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) |
0.00975 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2024-10-29 21:08:56 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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