Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g05330 | A04 | 3421841 | C | T | upstream_gene_variant | MODIFIER | c.-2525C>T| |
S84 S93 |
2 | BAA04g05330 | A04 | 3426604 | C | T | intron_variant | MODIFIER | c.278+1961C>T| |
S20 |
3 | BAA04g05330 | A04 | 3427799 | G | A | intron_variant | MODIFIER | c.278+3156G>A| |
S129 |
4 | BAA04g05330 | A04 | 3427962 | T | A | intron_variant | MODIFIER | c.278+3319T>A| |
S63 |
5 | BAA04g05330 | A04 | 3428198 | G | A | intron_variant | MODIFIER | c.278+3555G>A| |
S277 |
6 | BAA04g05330 | A04 | 3428712 | C | T | intron_variant | MODIFIER | c.278+4069C>T| |
S295 |
7 | BAA04g05330 | A04 | 3428997 | G | A | intron_variant | MODIFIER | c.278+4354G>A| |
S51 |
8 | BAA04g05330 | A04 | 3430281 | C | T | intron_variant | MODIFIER | c.279-3656C>T| |
S82 S92 |
9 | BAA04g05330 | A04 | 3430705 | C | T | intron_variant | MODIFIER | c.279-3232C>T| |
S289 S290 |
10 | BAA04g05330 | A04 | 3430920 | C | T | intron_variant | MODIFIER | c.279-3017C>T| |
S95 |
11 | BAA04g05330 | A04 | 3431403 | G | A | intron_variant | MODIFIER | c.279-2534G>A| |
S40 S49 |
12 | BAA04g05330 | A04 | 3432383 | C | T | intron_variant | MODIFIER | c.279-1554C>T| |
S23 |
13 | BAA04g05330 | A04 | 3433168 | G | A | intron_variant | MODIFIER | c.279-769G>A| |
S211 |
14 | BAA04g05330 | A04 | 3433733 | C | T | intron_variant | MODIFIER | c.279-204C>T| |
S98 |
15 | BAA04g05330 | A04 | 3434157 | C | T | missense_variant | MODERATE | c.499C>T|p.Pro167Ser |
S230 |
16 | BAA04g05330 | A04 | 3434365 | C | T | missense_variant | MODERATE | c.707C>T|p.Ser236Leu |
S152 |
17 | BAA04g05330 | A04 | 3434706 | C | T | missense_variant | MODERATE | c.1048C>T|p.Pro350Ser |
S23 |
18 | BAA04g05330 | A04 | 3434722 | G | A | missense_variant | MODERATE | c.1064G>A|p.Ser355Asn |
S79 S91 |
19 | BAA04g05330 | A04 | 3434726 | C | T | synonymous_variant | LOW | c.1068C>T|p.Ser356Ser |
S294 |
20 | BAA04g05330 | A04 | 3435114 | C | T | missense_variant | MODERATE | c.1456C>T|p.Pro486Ser |
S240 |
21 | BAA04g05330 | A04 | 3435587 | C | T | synonymous_variant | LOW | c.1929C>T|p.Tyr643Tyr |
S152 |
22 | BAA04g05330 | A04 | 3436396 | C | T | downstream_gene_variant | MODIFIER | c.*599C>T| |
S159 S299 |
23 | BAA04g05330 | A04 | 3436799 | G | A | downstream_gene_variant | MODIFIER | c.*1002G>A| |
S126 |
24 | BAA04g05330 | A04 | 3437274 | C | T | downstream_gene_variant | MODIFIER | c.*1477C>T| |
S239 S33 |
25 | BAA04g05330 | A04 | 3437777 | G | A | downstream_gene_variant | MODIFIER | c.*1980G>A| |
S75 S81 |