| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123701 | BAA10g13590 | A10 | 14589164 | G | A | upstream_gene_variant | MODIFIER | c.-521G>A| |
S179 |
| 123702 | BAA10g13590 | A10 | 14590603 | C | T | missense_variant | MODERATE | c.607C>T|p.Leu203Phe |
S104 S52 |
| 123703 | BAA10g13600 | A10 | 14592052 | C | T | missense_variant | MODERATE | c.1117G>A|p.Gly373Arg |
S104 S52 |
| 123704 | BAA10g13600 | A10 | 14592073 | C | T | missense_variant | MODERATE | c.1096G>A|p.Ala366Thr |
S137 S45 |
| 123705 | BAA10g13600 | A10 | 14592175 | G | A | missense_variant | MODERATE | c.994C>T|p.Pro332Ser |
S217 S248 |
| 123706 | BAA10g13600 | A10 | 14592479 | G | A | synonymous_variant | LOW | c.690C>T|p.Ile230Ile |
S295 |
| 123707 | BAA10g13600 | A10 | 14592611 | G | A | missense_variant | MODERATE | c.632C>T|p.Ala211Val |
S236 |
| 123708 | BAA10g13600 | A10 | 14592854 | C | T | missense_variant | MODERATE | c.389G>A|p.Gly130Glu |
S230 S26 |
| 123709 | BAA10g13600 | A10 | 14593126 | G | A | synonymous_variant | LOW | c.117C>T|p.Thr39Thr |
S43 |
| 123710 | BAA10g13600 | A10 | 14593235 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Phe |
S164 |
| 123711 | BAA10g13600 | A10 | 14593799 | G | A | upstream_gene_variant | MODIFIER | c.-557C>T| |
S127 |
| 123712 | BAA10g13600 | A10 | 14594504 | C | T | upstream_gene_variant | MODIFIER | c.-1262G>A| |
S116 |
| 123713 | BAA10g13600 | A10 | 14594939 | C | T | upstream_gene_variant | MODIFIER | c.-1697G>A| |
S116 |
| 123714 | BAA10g13600 | A10 | 14596180 | G | A | upstream_gene_variant | MODIFIER | c.-2938C>T| |
S175 |
| 123715 | BAA10g13600 | A10 | 14597099 | C | T | upstream_gene_variant | MODIFIER | c.-3857G>A| |
S122 |
| 123716 | BAA10g13610 | A10 | 14598337 | G | A | downstream_gene_variant | MODIFIER | c.*226C>T| |
S118 |
| 123717 | BAA10g13620 | A10 | 14599055 | G | A | downstream_gene_variant | MODIFIER | c.*3573C>T| |
S18 |
| 123718 | BAA10g13610 | A10 | 14599229 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1554-1G>A| |
S79 S91 |
| 123719 | BAA10g13620 | A10 | 14599467 | C | T | downstream_gene_variant | MODIFIER | c.*3161G>A| |
S298 |
| 123720 | BAA10g13620 | A10 | 14600352 | C | T | downstream_gene_variant | MODIFIER | c.*2276G>A| |
S308 |
| 123721 | BAA10g13610 | A10 | 14600568 | C | T | missense_variant | MODERATE | c.989G>A|p.Gly330Glu |
S236 |
| 123722 | BAA10g13610 | A10 | 14600607 | G | A | missense_variant | MODERATE | c.950C>T|p.Ser317Leu |
S286 |
| 123723 | BAA10g13620 | A10 | 14600853 | C | T | downstream_gene_variant | MODIFIER | c.*1775G>A| |
S167 |
| 123724 | BAA10g13610 | A10 | 14601555 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S280 |
| 123725 | BAA10g13610 | A10 | 14601803 | G | A | synonymous_variant | LOW | c.186C>T|p.Val62Val |
S195 |