Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20470 | A05 | 12614207 | G | A | synonymous_variant | LOW | c.2658C>T|p.Leu886Leu |
S148 S210 |
2 | BAA05g20470 | A05 | 12614233 | G | A | stop_gained | HIGH | c.2632C>T|p.Gln878* |
S218 |
3 | BAA05g20470 | A05 | 12614340 | G | A | missense_variant | MODERATE | c.2525C>T|p.Ala842Val |
S282 |
4 | BAA05g20470 | A05 | 12614494 | C | T | missense_variant | MODERATE | c.2458G>A|p.Val820Met |
S136 |
5 | BAA05g20470 | A05 | 12614716 | G | A | missense_variant | MODERATE | c.2236C>T|p.Pro746Ser |
S77 S82 |
6 | BAA05g20470 | A05 | 12615112 | C | T | missense_variant | MODERATE | c.1840G>A|p.Gly614Arg |
S211 |
7 | BAA05g20470 | A05 | 12615288 | C | T | missense_variant | MODERATE | c.1664G>A|p.Arg555Gln |
S261 |
8 | BAA05g20470 | A05 | 12616836 | G | A | intron_variant | MODIFIER | c.1616-1500C>T| |
S252 |
9 | BAA05g20470 | A05 | 12617085 | C | T | intron_variant | MODIFIER | c.1616-1749G>A| |
S100 |
10 | BAA05g20470 | A05 | 12617160 | C | T | intron_variant | MODIFIER | c.1615+1687G>A| |
S137 S215 |
11 | BAA05g20470 | A05 | 12617832 | G | A | intron_variant | MODIFIER | c.1615+1015C>T| |
S306 |
12 | BAA05g20470 | A05 | 12618030 | C | T | intron_variant | MODIFIER | c.1615+817G>A| |
S105 S106 |
13 | BAA05g20470 | A05 | 12618637 | G | A | intron_variant | MODIFIER | c.1615+210C>T| |
S107 |
14 | BAA05g20470 | A05 | 12619390 | C | T | splice_region_variant&intron_variant | LOW | c.1310+4G>A| |
S75 S81 |
15 | BAA05g20470 | A05 | 12619473 | C | T | missense_variant | MODERATE | c.1231G>A|p.Glu411Lys |
S268 |
16 | BAA05g20470 | A05 | 12619847 | A | T | missense_variant | MODERATE | c.1026T>A|p.Asp342Glu |
S112 |
17 | BAA05g20470 | A05 | 12619962 | C | T | missense_variant | MODERATE | c.911G>A|p.Arg304Lys |
S306 |
18 | BAA05g20470 | A05 | 12620184 | G | A | missense_variant | MODERATE | c.772C>T|p.Leu258Phe |
S75 S81 |
19 | BAA05g20470 | A05 | 12620438 | C | T | splice_region_variant&intron_variant | LOW | c.609+6G>A| |
S287 S85 |
20 | BAA05g20470 | A05 | 12620943 | G | A | missense_variant | MODERATE | c.220C>T|p.Leu74Phe |
S82 S92 |
21 | BAA05g20470 | A05 | 12621133 | G | A | synonymous_variant | LOW | c.30C>T|p.Ala10Ala |
S187 |
22 | BAA05g20470 | A05 | 12621827 | C | T | upstream_gene_variant | MODIFIER | c.-665G>A| |
S84 S93 |
23 | BAA05g20470 | A05 | 12621952 | C | T | upstream_gene_variant | MODIFIER | c.-790G>A| |
S103 |
24 | BAA05g20470 | A05 | 12622094 | C | T | upstream_gene_variant | MODIFIER | c.-932G>A| |
S202 |
25 | BAA05g20470 | A05 | 12622377 | G | A | upstream_gene_variant | MODIFIER | c.-1215C>T| |
S293 |