Variant #0000567284 (NC_000019.9:g.39219082_39219090dup, NC_000019.9(NM_004924.4):c.2418+416_2418+424dup (ACTN4))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.39219082_39219090dup |
| DNA change (hg38) |
g.38728442_38728450dup |
| Published as |
ACTN4(NM_004924.6):c.2418+410_2418+418dupTCCTCCTCC, ACTN4(NM_004924.6):c.2418+413_2418+421dupTCCTCCTCC |
| ISCN |
- |
| DB-ID |
ACTN4_000026 |
| 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
|