Variant #0000621211 (NC_000003.11:g.167512399_167512405del, NC_000003.11(NM_001122752.1):c.677-9_677-3del (SERPINI1))
| Chromosome |
3 |
| 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.167512399_167512405del |
| DNA change (hg38) |
g.167794611_167794617del |
| Published as |
SERPINI1(NM_005025.4):c.677-9_677-3delTCTTTTT |
| ISCN |
- |
| DB-ID |
SERPINI1_000016 |
| 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 |
2019-12-06 12:43:26 +01:00 (CET) |
| Date last edited |
2020-06-15 16:53:48 +02:00 (CEST) |

Variant on transcripts
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