Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37150 | A02 | 31797181 | G | A | downstream_gene_variant | MODIFIER | c.*4289C>T| |
S237 |
2 | BAA02g37150 | A02 | 31797615 | G | A | downstream_gene_variant | MODIFIER | c.*3855C>T| |
S13 |
3 | BAA02g37150 | A02 | 31797620 | G | A | downstream_gene_variant | MODIFIER | c.*3850C>T| |
S185 |
4 | BAA02g37150 | A02 | 31797730 | G | A | downstream_gene_variant | MODIFIER | c.*3740C>T| |
S67 |
5 | BAA02g37150 | A02 | 31798688 | C | T | downstream_gene_variant | MODIFIER | c.*2782G>A| |
S193 |
6 | BAA02g37150 | A02 | 31798797 | G | A | downstream_gene_variant | MODIFIER | c.*2673C>T| |
S58 |
7 | BAA02g37150 | A02 | 31799056 | G | A | downstream_gene_variant | MODIFIER | c.*2414C>T| |
S34 |
8 | BAA02g37150 | A02 | 31799506 | C | T | downstream_gene_variant | MODIFIER | c.*1964G>A| |
S65 |
9 | BAA02g37150 | A02 | 31799634 | G | A | downstream_gene_variant | MODIFIER | c.*1836C>T| |
S136 |
10 | BAA02g37150 | A02 | 31799980 | C | T | downstream_gene_variant | MODIFIER | c.*1490G>A| |
S181 |
11 | BAA02g37150 | A02 | 31800557 | G | A | downstream_gene_variant | MODIFIER | c.*913C>T| |
S239 |
12 | BAA02g37150 | A02 | 31801518 | C | T | stop_gained | HIGH | c.1434G>A|p.Trp478* |
S244 |
13 | BAA02g37150 | A02 | 31801725 | C | T | synonymous_variant | LOW | c.1227G>A|p.Ala409Ala |
S25 |
14 | BAA02g37150 | A02 | 31802115 | C | T | missense_variant | MODERATE | c.968G>A|p.Ser323Asn |
S250 |
15 | BAA02g37150 | A02 | 31802237 | G | A | synonymous_variant | LOW | c.954C>T|p.Phe318Phe |
S60 |
16 | BAA02g37150 | A02 | 31802588 | C | T | synonymous_variant | LOW | c.690G>A|p.Glu230Glu |
S53 |
17 | BAA02g37150 | A02 | 31802624 | G | A | synonymous_variant | LOW | c.654C>T|p.Phe218Phe |
S232 |
18 | BAA02g37150 | A02 | 31802650 | G | A | missense_variant | MODERATE | c.628C>T|p.Leu210Phe |
S13 S140 S219 S279 S64 S72 |
19 | BAA02g37150 | A02 | 31803179 | G | A | missense_variant | MODERATE | c.332C>T|p.Pro111Leu |
S126 |
20 | BAA02g37150 | A02 | 31803180 | G | A | missense_variant | MODERATE | c.331C>T|p.Pro111Ser |
S35 |
21 | BAA02g37150 | A02 | 31804366 | C | T | upstream_gene_variant | MODIFIER | c.-474G>A| |
S299 |
22 | BAA02g37150 | A02 | 31804519 | G | A | upstream_gene_variant | MODIFIER | c.-627C>T| |
S34 |
23 | BAA02g37150 | A02 | 31805600 | C | T | upstream_gene_variant | MODIFIER | c.-1708G>A| |
S18 |
24 | BAA02g37150 | A02 | 31805654 | G | A | upstream_gene_variant | MODIFIER | c.-1762C>T| |
S256 |
25 | BAA02g37150 | A02 | 31807148 | C | T | upstream_gene_variant | MODIFIER | c.-3256G>A| |
S109 |