Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13130 | A05 | 6785469 | G | A | missense_variant | MODERATE | c.685G>A|p.Val229Ile |
S243 S299 |
2 | BAA05g13130 | A05 | 6785658 | C | T | stop_gained | HIGH | c.874C>T|p.Gln292* |
S207 |
3 | BAA05g13130 | A05 | 6785983 | G | A | missense_variant | MODERATE | c.1199G>A|p.Gly400Asp |
S210 |
4 | BAA05g13130 | A05 | 6785990 | G | A | synonymous_variant | LOW | c.1206G>A|p.Val402Val |
S208 S219 |
5 | BAA05g13130 | A05 | 6786198 | G | A | missense_variant | MODERATE | c.1414G>A|p.Glu472Lys |
S296 |
6 | BAA05g13130 | A05 | 6786496 | G | A | downstream_gene_variant | MODIFIER | c.*17G>A| |
S37 |
7 | BAA05g13130 | A05 | 6787007 | G | A | downstream_gene_variant | MODIFIER | c.*528G>A| |
S62 |
8 | BAA05g13130 | A05 | 6787227 | C | T | downstream_gene_variant | MODIFIER | c.*748C>T| |
S164 |
9 | BAA05g13130 | A05 | 6787427 | C | T | downstream_gene_variant | MODIFIER | c.*948C>T| |
S155 |
10 | BAA05g13130 | A05 | 6789098 | G | A | downstream_gene_variant | MODIFIER | c.*2619G>A| |
S170 |
11 | BAA05g13130 | A05 | 6789187 | C | T | downstream_gene_variant | MODIFIER | c.*2708C>T| |
S85 |
12 | BAA05g13130 | A05 | 6789205 | G | A | downstream_gene_variant | MODIFIER | c.*2726G>A| |
S46 |
13 | BAA05g13130 | A05 | 6789446 | G | A | downstream_gene_variant | MODIFIER | c.*2967G>A| |
S224 S6 |
14 | BAA05g13130 | A05 | 6789579 | G | A | downstream_gene_variant | MODIFIER | c.*3100G>A| |
S178 |
15 | BAA05g13130 | A05 | 6789600 | G | A | downstream_gene_variant | MODIFIER | c.*3121G>A| |
S129 |
16 | BAA05g13130 | A05 | 6789976 | C | T | downstream_gene_variant | MODIFIER | c.*3497C>T| |
S197 |
17 | BAA05g13130 | A05 | 6790372 | C | T | downstream_gene_variant | MODIFIER | c.*3893C>T| |
S270 |