Variant #0000534643 (NC_000008.10:g.27637708_27637709del, NM_001017420.2:c.879_880del (ESCO2))
| Chromosome |
8 |
| 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.27637708_27637709del |
| DNA change (hg38) |
g.27780191_27780192del |
| Published as |
ESCO2(NM_001017420.2):c.879_880delAG (p.R293Sfs*7), ESCO2(NM_001017420.3):c.879_880delAG (p.R293Sfs*7) |
| ISCN |
- |
| DB-ID |
ESCO2_000050 See all 2 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| 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
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