Variant #0000321129 (NC_000001.10:g.173797451T>C, NC_000001.10(NM_018122.4):c.228-20T>C (DARS2))
| Chromosome |
1 |
| 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.173797451T>C |
| DNA change (hg38) |
g.173828313T>C |
| Published as |
DARS2(NM_018122.4):c.228-20delinsC (p.(=)), DARS2(NM_018122.5):c.228-20T>C |
| ISCN |
- |
| DB-ID |
DARS2_000002 See all 7 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) |
0.27229 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|