Variant #0000570798 (NC_000021.8:g.45750687_45750696dup, NC_000021.8(NM_004928.2):c.642+17_642+26dup (C21orf2))
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45750687_45750696dup |
| DNA change (hg38) |
g.44330804_44330813dup |
| Published as |
CFAP410(NM_001271441.2):c.656_665dup (p.(Ala223ArgfsTer38)), CFAP410(NM_001271441.2):c.656_665dupTAGGGGCCGC (p.A223Rfs*38) |
| ISCN |
- |
| DB-ID |
C21orf2_000029 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) |
Retrieve |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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