Variant #0000950698 (NC_000016.9:g.67692466_67692477del, NM_022914.2:c.1066_1077del (ACD))
| Chromosome |
16 |
| 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.67692466_67692477del |
| DNA change (hg38) |
- |
| Published as |
ACD(NM_001082486.2):c.817_828delCCCAGTTCCTCA (p.P273_S276del) |
| ISCN |
- |
| DB-ID |
ACD_000015 See all 3 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_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2023-11-27 17:35:39 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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