Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g24960 | A01 | 13361154 | G | A | missense_variant | MODERATE | c.1061C>T|p.Pro354Leu |
S252 |
2 | BAA01g24960 | A01 | 13361377 | G | A | intron_variant | MODIFIER | c.985-12C>T| |
S72 S78 |
3 | BAA01g24960 | A01 | 13361485 | G | A | synonymous_variant | LOW | c.957C>T|p.Ala319Ala |
S13 S140 S64 |
4 | BAA01g24960 | A01 | 13361980 | G | A | missense_variant | MODERATE | c.731C>T|p.Ser244Phe |
S159 S243 S276 S298 S299 |
5 | BAA01g24960 | A01 | 13362240 | C | T | missense_variant | MODERATE | c.560G>A|p.Arg187Lys |
S159 S243 |
6 | BAA01g24960 | A01 | 13362371 | G | A | intron_variant | MODIFIER | c.522+23C>T| |
S2 |
7 | BAA01g24960 | A01 | 13362460 | G | A | synonymous_variant | LOW | c.456C>T|p.Asp152Asp |
S240 |
8 | BAA01g24960 | A01 | 13362545 | G | A | missense_variant | MODERATE | c.371C>T|p.Pro124Leu |
S202 |
9 | BAA01g24960 | A01 | 13363076 | G | A | intron_variant | MODIFIER | c.197+60C>T| |
S263 |
10 | BAA01g24960 | A01 | 13363779 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S104 S52 |
11 | BAA01g24960 | A01 | 13363898 | G | A | upstream_gene_variant | MODIFIER | c.-566C>T| |
S207 |
12 | BAA01g24960 | A01 | 13364820 | C | T | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S242 |
13 | BAA01g24960 | A01 | 13365537 | C | T | upstream_gene_variant | MODIFIER | c.-2205G>A| |
S128 |
14 | BAA01g24960 | A01 | 13366693 | C | T | upstream_gene_variant | MODIFIER | c.-3361G>A| |
S44 |
15 | BAA01g24960 | A01 | 13366936 | C | T | upstream_gene_variant | MODIFIER | c.-3604G>A| |
S61 |