Variant #0000339670 (NC_000005.9:g.218387dup, NM_004168.2:c.-84dup (SDHA))
| Chromosome |
5 |
| 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.218387dup |
| DNA change (hg38) |
g.218272dup |
| Published as |
SDHA:NM_004168.2:c.-84dup (=) |
| ISCN |
- |
| DB-ID |
SDHA_000111 |
| Variant remarks |
VKGL data sharing initiative Nederland; Variant no longer found in the VKGL dataset for this center. |
| 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_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2026-01-21 10:43:54 +01:00 (CET) |

Variant on transcripts
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