Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12770 | A05 | 6575752 | G | A | downstream_gene_variant | MODIFIER | c.*2770C>T| |
S298 |
2 | BAA05g12770 | A05 | 6578565 | C | T | missense_variant | MODERATE | c.2807G>A|p.Gly936Glu |
S61 |
3 | BAA05g12770 | A05 | 6578586 | G | A | missense_variant | MODERATE | c.2786C>T|p.Pro929Leu |
S200 |
4 | BAA05g12770 | A05 | 6578611 | C | T | missense_variant&splice_region_variant | MODERATE | c.2761G>A|p.Ala921Thr |
S104 S52 |
5 | BAA05g12770 | A05 | 6578734 | G | A | missense_variant | MODERATE | c.2704C>T|p.Arg902Cys |
S293 |
6 | BAA05g12770 | A05 | 6579018 | G | A | missense_variant | MODERATE | c.2420C>T|p.Thr807Ile |
S107 |
7 | BAA05g12770 | A05 | 6579158 | G | A | synonymous_variant | LOW | c.2280C>T|p.Ile760Ile |
S4 |
8 | BAA05g12770 | A05 | 6579258 | C | T | missense_variant | MODERATE | c.2180G>A|p.Gly727Glu |
S157 |
9 | BAA05g12770 | A05 | 6580435 | G | A | missense_variant | MODERATE | c.1237C>T|p.Arg413Cys |
S187 |
10 | BAA05g12770 | A05 | 6580612 | C | T | missense_variant | MODERATE | c.1060G>A|p.Ala354Thr |
S167 |
11 | BAA05g12770 | A05 | 6580981 | C | T | missense_variant | MODERATE | c.691G>A|p.Ala231Thr |
S153 S213 |
12 | BAA05g12770 | A05 | 6581068 | C | T | missense_variant | MODERATE | c.604G>A|p.Asp202Asn |
S18 |
13 | BAA05g12770 | A05 | 6581148 | C | T | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S182 |
14 | BAA05g12770 | A05 | 6581530 | C | T | missense_variant | MODERATE | c.142G>A|p.Val48Ile |
S89 |
15 | BAA05g12770 | A05 | 6581781 | G | A | upstream_gene_variant | MODIFIER | c.-110C>T| |
S279 |
16 | BAA05g12770 | A05 | 6582493 | G | A | upstream_gene_variant | MODIFIER | c.-822C>T| |
S70 |
17 | BAA05g12770 | A05 | 6583289 | G | A | upstream_gene_variant | MODIFIER | c.-1618C>T| |
S150 |
18 | BAA05g12770 | A05 | 6584456 | G | A | upstream_gene_variant | MODIFIER | c.-2785C>T| |
S13 |
19 | BAA05g12770 | A05 | 6585871 | C | T | upstream_gene_variant | MODIFIER | c.-4200G>A| |
S44 |