Variant #0000895451 (NC_000021.8:g.33043786_33043787del, NM_020706.2:c.3371_3372del (SCAF4))
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.33043786_33043787del |
| DNA change (hg38) |
- |
| Published as |
SCAF4(NM_020706.2):c.3371_3372delAG (p.E1124Vfs*4) |
| ISCN |
- |
| DB-ID |
SOD1_000028 |
| 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 |
2022-11-01 13:41:49 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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