Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29410 | A10 | 22141131 | G | A | synonymous_variant | LOW | c.1869C>T|p.Phe623Phe |
S235 |
2 | BAA10g29410 | A10 | 22141758 | C | T | splice_region_variant&intron_variant | LOW | c.1699+5G>A| |
S108 S72 |
3 | BAA10g29410 | A10 | 22142553 | G | A | missense_variant | MODERATE | c.1363C>T|p.Leu455Phe |
S132 S137 S138 S215 |
4 | BAA10g29410 | A10 | 22142558 | G | A | missense_variant | MODERATE | c.1358C>T|p.Pro453Leu |
S303 |
5 | BAA10g29410 | A10 | 22142559 | G | A | missense_variant | MODERATE | c.1357C>T|p.Pro453Ser |
S265 |
6 | BAA10g29410 | A10 | 22143176 | G | A | missense_variant | MODERATE | c.1052C>T|p.Thr351Ile |
S39 |
7 | BAA10g29410 | A10 | 22143438 | G | A | synonymous_variant | LOW | c.925C>T|p.Leu309Leu |
S271 |
8 | BAA10g29410 | A10 | 22143702 | G | A | stop_gained | HIGH | c.886C>T|p.Gln296* |
S212 |
9 | BAA10g29410 | A10 | 22143977 | C | T | missense_variant | MODERATE | c.752G>A|p.Arg251Lys |
S68 |
10 | BAA10g29410 | A10 | 22145515 | C | T | missense_variant | MODERATE | c.11G>A|p.Gly4Glu |
S275 |
11 | BAA10g29410 | A10 | 22150167 | C | T | upstream_gene_variant | MODIFIER | c.-4642G>A| |
S25 |