Variant #0000341279 (NC_000016.9:g.89346164dup, NM_013275.5:c.6792dup (ANKRD11))
| Chromosome |
16 |
| 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.89346164dup |
| DNA change (hg38) |
g.89279756dup |
| Published as |
ANKRD11(NM_001256182.1):c.6792dupC (p.A2265Rfs*8), ANKRD11(NM_013275.5):c.6792dupC (p.(Ala2265fs)), ANKRD11(NM_013275.6):c.6792dupC (p.A2265Rfs*8) |
| ISCN |
- |
| DB-ID |
ANKRD11_000096 See all 7 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_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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