Variant #0000804983 (NC_000011.9:g.125875967_125875970del, NC_000011.9(NM_016952.4):c.1553-11_1553-8del (CDON))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.125875967_125875970del |
| DNA change (hg38) |
- |
| Published as |
CDON(NM_001243597.1):c.1553-11_1553-8delTCTC, CDON(NM_001378964.1):c.1553-11_1553-8delTCTC |
| ISCN |
- |
| DB-ID |
CDON_000069 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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