Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16860 | A01 | 8178489 | C | T | upstream_gene_variant | MODIFIER | c.-3948C>T| |
S182 |
2 | BAA01g16860 | A01 | 8178794 | G | A | upstream_gene_variant | MODIFIER | c.-3643G>A| |
S104 |
3 | BAA01g16860 | A01 | 8180857 | G | A | upstream_gene_variant | MODIFIER | c.-1580G>A| |
S149 |
4 | BAA01g16860 | A01 | 8180859 | G | A | upstream_gene_variant | MODIFIER | c.-1578G>A| |
S193 |
5 | BAA01g16860 | A01 | 8181078 | G | A | upstream_gene_variant | MODIFIER | c.-1359G>A| |
S60 |
6 | BAA01g16860 | A01 | 8181827 | G | A | upstream_gene_variant | MODIFIER | c.-610G>A| |
S174 |
7 | BAA01g16860 | A01 | 8182783 | G | A | missense_variant | MODERATE | c.347G>A|p.Arg116Lys |
S278 |
8 | BAA01g16860 | A01 | 8182943 | G | A | missense_variant&splice_region_variant | MODERATE | c.425G>A|p.Gly142Asp |
S238 |
9 | BAA01g16860 | A01 | 8183008 | G | A | missense_variant | MODERATE | c.490G>A|p.Ala164Thr |
S247 |
10 | BAA01g16860 | A01 | 8183634 | G | A | missense_variant | MODERATE | c.743G>A|p.Gly248Glu |
S34 |
11 | BAA01g16860 | A01 | 8184281 | C | T | intron_variant | MODIFIER | c.997-56C>T| |
S215 |
12 | BAA01g16860 | A01 | 8184311 | C | T | intron_variant | MODIFIER | c.997-26C>T| |
S179 |
13 | BAA01g16860 | A01 | 8185094 | G | A | missense_variant | MODERATE | c.1393G>A|p.Asp465Asn |
S240 |
14 | BAA01g16860 | A01 | 8185363 | G | A | intron_variant | MODIFIER | c.1508-38G>A| |
S13 |
15 | BAA01g16860 | A01 | 8185470 | C | T | missense_variant | MODERATE | c.1577C>T|p.Ser526Phe |
S206 S26 |
16 | BAA01g16860 | A01 | 8185543 | C | T | intron_variant | MODIFIER | c.1619+31C>T| |
S158 |
17 | BAA01g16860 | A01 | 8185867 | C | T | missense_variant | MODERATE | c.1781C>T|p.Pro594Leu |
S192 |
18 | BAA01g16860 | A01 | 8186337 | C | T | intron_variant | MODIFIER | c.2007+86C>T| |
S130 |
19 | BAA01g16860 | A01 | 8188939 | C | T | missense_variant | MODERATE | c.2261C>T|p.Ser754Leu |
S140 |
20 | BAA01g16860 | A01 | 8191368 | C | T | downstream_gene_variant | MODIFIER | c.*1233C>T| |
S289 S290 |
21 | BAA01g16860 | A01 | 8192161 | C | T | downstream_gene_variant | MODIFIER | c.*2026C>T| |
S231 |