| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 147601 | BAA10g31920 | A10 | 23149347 | G | A | upstream_gene_variant | MODIFIER | c.-3590C>T| |
S88 |
| 147602 | BAA10g31950 | A10 | 23149889 | C | T | missense_variant&splice_region_variant | MODERATE | c.1652G>A|p.Ser551Asn |
S236 |
| 147603 | BAA10g31950 | A10 | 23149923 | G | A | missense_variant | MODERATE | c.1618C>T|p.His540Tyr |
S89 |
| 147604 | BAA10g31940 | A10 | 23152621 | G | A | upstream_gene_variant | MODIFIER | c.-3601C>T| |
S219 S72 |
| 147605 | BAA10g31950 | A10 | 23152756 | G | A | missense_variant | MODERATE | c.385C>T|p.Arg129Cys |
S276 |
| 147606 | BAA10g31950 | A10 | 23156048 | C | T | upstream_gene_variant | MODIFIER | c.-2277G>A| |
S244 |
| 147607 | BAA10g31960 | A10 | 23156868 | G | A | missense_variant | MODERATE | c.805C>T|p.Leu269Phe |
S50 |
| 147608 | BAA10g31960 | A10 | 23157356 | C | T | missense_variant | MODERATE | c.464G>A|p.Arg155Lys |
S283 |
| 147609 | BAA10g31950 | A10 | 23158016 | C | T | upstream_gene_variant | MODIFIER | c.-4245G>A| |
S130 |
| 147610 | BAA10g31960 | A10 | 23158284 | G | A | synonymous_variant | LOW | c.96C>T|p.Leu32Leu |
S64 |
| 147611 | BAA10g31960 | A10 | 23158376 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S299 |
| 147612 | BAA10g31970 | A10 | 23160817 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S280 |
| 147613 | BAA10g31960 | A10 | 23161049 | C | T | upstream_gene_variant | MODIFIER | c.-2670G>A| |
S206 S26 |
| 147614 | BAA10g31960 | A10 | 23161056 | G | A | upstream_gene_variant | MODIFIER | c.-2677C>T| |
S111 |
| 147615 | BAA10g31960 | A10 | 23161447 | C | T | upstream_gene_variant | MODIFIER | c.-3068G>A| |
S276 |
| 147616 | BAA10g31970 | A10 | 23163750 | G | A | upstream_gene_variant | MODIFIER | c.-2755C>T| |
S4 |
| 147617 | BAA10g31980 | A10 | 23163975 | C | T | missense_variant | MODERATE | c.874G>A|p.Glu292Lys |
S161 |
| 147618 | BAA10g31980 | A10 | 23164359 | C | T | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S18 |
| 147619 | BAA10g31980 | A10 | 23164383 | C | T | missense_variant | MODERATE | c.466G>A|p.Val156Ile |
S301 S304 |
| 147620 | BAA10g31980 | A10 | 23164515 | C | T | missense_variant | MODERATE | c.334G>A|p.Ala112Thr |
S139 |
| 147621 | BAA10g31980 | A10 | 23164633 | C | T | synonymous_variant | LOW | c.216G>A|p.Gly72Gly |
S11 |
| 147622 | BAA10g31980 | A10 | 23164837 | G | A | synonymous_variant | LOW | c.12C>T|p.Tyr4Tyr |
S63 |
| 147623 | BAA10g31970 | A10 | 23165323 | C | T | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S103 |
| 147624 | BAA10g31980 | A10 | 23167886 | C | T | upstream_gene_variant | MODIFIER | c.-3038G>A| |
S281 |
| 147625 | BAA10g31980 | A10 | 23168292 | C | T | upstream_gene_variant | MODIFIER | c.-3444G>A| |
S187 |