Variant #0000575762 (NC_000023.10:g.36322055G>C, NM_001304548.1:c.8062G>C (CXorf59))
| Chromosome |
X |
| 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.36322055G>C |
| DNA change (hg38) |
g.36303940G>C |
| Published as |
CFAP47(NM_001304548.1):c.8062G>C (p.D2688H), CFAP47(NM_001304548.2):c.8062G>C (p.D2688H) |
| ISCN |
- |
| DB-ID |
CXorf59_000017 See all 2 reported entries |
| 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) |
0.00101 View details |
| 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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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