Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g31570 | A09 | 39558345 | G | A | upstream_gene_variant | MODIFIER | c.-4778G>A| |
S282 |
2 | BAA09g31570 | A09 | 39558997 | T | C | upstream_gene_variant | MODIFIER | c.-4126T>C| |
S245 |
3 | BAA09g31570 | A09 | 39559127 | G | T | upstream_gene_variant | MODIFIER | c.-3996G>T| |
S175 S218 S281 S62 S66 |
4 | BAA09g31570 | A09 | 39559134 | C | A | upstream_gene_variant | MODIFIER | c.-3989C>A| |
S147 S175 S206 S223 S229 S32 S38 S66 |
5 | BAA09g31570 | A09 | 39559908 | C | T | upstream_gene_variant | MODIFIER | c.-3215C>T| |
S245 |
6 | BAA09g31570 | A09 | 39559954 | C | T | upstream_gene_variant | MODIFIER | c.-3169C>T| |
S187 |
7 | BAA09g31570 | A09 | 39560375 | G | A | upstream_gene_variant | MODIFIER | c.-2748G>A| |
S46 |
8 | BAA09g31570 | A09 | 39561036 | G | A | upstream_gene_variant | MODIFIER | c.-2087G>A| |
S111 |
9 | BAA09g31570 | A09 | 39562278 | C | T | upstream_gene_variant | MODIFIER | c.-845C>T| |
S188 |
10 | BAA09g31570 | A09 | 39562520 | C | T | upstream_gene_variant | MODIFIER | c.-603C>T| |
S180 |
11 | BAA09g31570 | A09 | 39562760 | C | T | upstream_gene_variant | MODIFIER | c.-363C>T| |
S233 |
12 | BAA09g31570 | A09 | 39562839 | C | T | upstream_gene_variant | MODIFIER | c.-284C>T| |
S182 |
13 | BAA09g31570 | A09 | 39563074 | C | T | upstream_gene_variant | MODIFIER | c.-49C>T| |
S256 |
14 | BAA09g31570 | A09 | 39563207 | C | T | missense_variant | MODERATE | c.85C>T|p.Pro29Ser |
S180 |
15 | BAA09g31570 | A09 | 39563289 | C | T | missense_variant | MODERATE | c.167C>T|p.Pro56Leu |
S152 |
16 | BAA09g31570 | A09 | 39563500 | C | T | synonymous_variant | LOW | c.378C>T|p.Ile126Ile |
S246 |
17 | BAA09g31570 | A09 | 39563529 | C | T | missense_variant | MODERATE | c.407C>T|p.Pro136Leu |
S192 |
18 | BAA09g31570 | A09 | 39564316 | C | T | synonymous_variant | LOW | c.1194C>T|p.Arg398Arg |
S23 |
19 | BAA09g31570 | A09 | 39564477 | C | T | missense_variant | MODERATE | c.1264C>T|p.Leu422Phe |
S168 |
20 | BAA09g31570 | A09 | 39564665 | G | A | synonymous_variant | LOW | c.1452G>A|p.Arg484Arg |
S87 |
21 | BAA09g31570 | A09 | 39564686 | C | T | synonymous_variant | LOW | c.1473C>T|p.Leu491Leu |
S255 |
22 | BAA09g31570 | A09 | 39566505 | G | A | missense_variant | MODERATE | c.1931G>A|p.Arg644Gln |
S302 |
23 | BAA09g31570 | A09 | 39566843 | G | A | synonymous_variant | LOW | c.2187G>A|p.Ser729Ser |
S217 S248 |