Variant #0000866118 (NC_000019.9:g.39406271_39406279dup, NM_017827.3:c.1530_1538dup (SARS2))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.39406271_39406279dup |
| DNA change (hg38) |
- |
| Published as |
SARS2(NM_001145901.1):c.1536_1544dupGCTGCCTGG (p.L513_G515dup), SARS2(NM_017827.4):c.1530_1538dupGCTGCCTGG (p.L511_G513dup) |
| ISCN |
- |
| DB-ID |
SARS2_000008 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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