Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g07780 | A06 | 4069259 | C | T | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S245 |
2 | BAA06g07780 | A06 | 4069417 | G | A | missense_variant | MODERATE | c.344G>A|p.Gly115Asp |
S283 |
3 | BAA06g07780 | A06 | 4069610 | C | T | missense_variant | MODERATE | c.454C>T|p.His152Tyr |
S134 |
4 | BAA06g07780 | A06 | 4070262 | G | A | missense_variant | MODERATE | c.733G>A|p.Asp245Asn |
S233 |
5 | BAA06g07780 | A06 | 4070409 | C | T | missense_variant | MODERATE | c.880C>T|p.Pro294Ser |
S259 |
6 | BAA06g07780 | A06 | 4070575 | C | T | synonymous_variant | LOW | c.945C>T|p.Asp315Asp |
S295 |
7 | BAA06g07780 | A06 | 4071929 | C | T | missense_variant | MODERATE | c.1948C>T|p.Pro650Ser |
S16 |
8 | BAA06g07780 | A06 | 4072061 | G | A | missense_variant | MODERATE | c.2080G>A|p.Asp694Asn |
S182 |
9 | BAA06g07780 | A06 | 4072760 | G | A | synonymous_variant | LOW | c.2538G>A|p.Lys846Lys |
S267 |
10 | BAA06g07780 | A06 | 4072812 | C | T | missense_variant | MODERATE | c.2590C>T|p.His864Tyr |
S296 |
11 | BAA06g07780 | A06 | 4073163 | G | A | synonymous_variant | LOW | c.2778G>A|p.Lys926Lys |
S35 |
12 | BAA06g07780 | A06 | 4073828 | G | A | downstream_gene_variant | MODIFIER | c.*308G>A| |
S208 S219 |
13 | BAA06g07780 | A06 | 4074317 | C | T | downstream_gene_variant | MODIFIER | c.*797C>T| |
S44 |
14 | BAA06g07780 | A06 | 4074454 | C | T | downstream_gene_variant | MODIFIER | c.*934C>T| |
S60 |