Variant #0000616934 (NC_000017.10:g.80405460_80405461del, NM_001033046.3:c.123_124del (C17orf62))
| Chromosome |
17 |
| 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.80405460_80405461del |
| DNA change (hg38) |
g.82447584_82447585del |
| Published as |
C17orf62(NM_001193653.1):c.123_124delCG (p.S41Rfs*3) |
| ISCN |
- |
| DB-ID |
C17orf62_000005 |
| 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 |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-14 16:09:25 +02:00 (CEST) |

Variant on transcripts
|