Variant #0000790065 (NC_000001.10:g.38620899_38620903dup)
| Individual ID |
00376452 |
| Chromosome |
1 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.38620899_38620903dup |
| DNA change (hg38) |
g.38579408_38579412dup |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr1_014321 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Chunli Wang |
| Database submission license |
Creative Commons Attribution-NoDerivatives 4.0 International |
| Created by |
Chunli Wang |
| Date created |
2021-06-23 04:12:12 +02:00 (CEST) |
| Date last edited |
2021-06-23 09:23:09 +02:00 (CEST) |

Variant on transcripts
Screenings
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