Table 3.
Truncating vs missense SDH variants.
| SDH subunit | Variant type | n (%)a | 
|---|---|---|
| A | Total | 83,641 (100%, 38.9%) | 
| Missense | 83,344 (99.6%, 38.8%) | |
| Truncating | 297 (0.4%, 0.14%) | |
| B | Total | 6536 (100%, 3.0%) | 
| Missense | 6133 (93.8%, 2.9%) | |
| Truncating | 403 (6.2%, 0.19%) | |
| C | Total | 2724 (100%, 1.3%) | 
| Missense | 2572 (94.4%, 1.2%) | |
| Truncating | 152 (5.6%, 0.07%) | |
| D | Total | 121,904 (100%,56.8%) | 
| Missense | 121,681 (99.8%, 56.6%) | |
| Truncating | 223 (0.2%, 0.1%) | 
Bold indicates highest truncating percentage in column
an, variants as number (percent for subunit, percent overall) of total genomes (214,805).
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