Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g34210 | A07 | 32762528 | G | A | upstream_gene_variant | MODIFIER | c.-3955G>A| |
S69 |
2 | BAA07g34210 | A07 | 32766552 | G | A | missense_variant | MODERATE | c.70G>A|p.Asp24Asn |
S172 S217 |
3 | BAA07g34210 | A07 | 32767161 | G | A | missense_variant | MODERATE | c.679G>A|p.Ala227Thr |
S18 |
4 | BAA07g34210 | A07 | 32767705 | C | T | missense_variant | MODERATE | c.1223C>T|p.Ala408Val |
S159 S243 |
5 | BAA07g34210 | A07 | 32767972 | G | A | missense_variant | MODERATE | c.1490G>A|p.Gly497Glu |
S158 |
6 | BAA07g34210 | A07 | 32768720 | G | A | synonymous_variant | LOW | c.2094G>A|p.Lys698Lys |
S205 |
7 | BAA07g34210 | A07 | 32769207 | G | A | missense_variant | MODERATE | c.2581G>A|p.Glu861Lys |
S126 |
8 | BAA07g34210 | A07 | 32769285 | G | A | missense_variant | MODERATE | c.2659G>A|p.Val887Met |
S136 |
9 | BAA07g34210 | A07 | 32769348 | G | A | missense_variant | MODERATE | c.2722G>A|p.Ala908Thr |
S239 |
10 | BAA07g34210 | A07 | 32769573 | G | A | missense_variant | MODERATE | c.2947G>A|p.Val983Ile |
S130 |
11 | BAA07g34210 | A07 | 32773260 | G | A | missense_variant&splice_region_variant | MODERATE | c.3328G>A|p.Glu1110Lys |
S38 |
12 | BAA07g34210 | A07 | 32773738 | C | T | missense_variant | MODERATE | c.3634C>T|p.Pro1212Ser |
S44 |
13 | BAA07g34210 | A07 | 32773856 | C | T | missense_variant | MODERATE | c.3752C>T|p.Thr1251Ile |
S169 |