Variant #0000289632 (NC_000015.9:g.41337180G>A, NM_017553.1:c.2829C>T (INO80))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41337180G>A |
| DNA change (hg38) |
g.41044982G>A |
| Published as |
INO80(NM_017553.3):c.2829C>T (p.Y943=) |
| ISCN |
- |
| DB-ID |
INO80_000001 |
| 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) |
0.00339 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-07-06 10:23:12 +02:00 (CEST) |

Variant on transcripts
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