Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06880 | A04 | 4549731 | G | A | downstream_gene_variant | MODIFIER | c.*2131C>T| |
S104 S52 |
2 | BAA04g06880 | A04 | 4550555 | C | T | downstream_gene_variant | MODIFIER | c.*1307G>A| |
S100 |
3 | BAA04g06880 | A04 | 4550760 | A | T | downstream_gene_variant | MODIFIER | c.*1102T>A| |
S36 |
4 | BAA04g06880 | A04 | 4550993 | G | A | downstream_gene_variant | MODIFIER | c.*869C>T| |
S62 |
5 | BAA04g06880 | A04 | 4551764 | G | A | downstream_gene_variant | MODIFIER | c.*98C>T| |
S69 |
6 | BAA04g06880 | A04 | 4551975 | C | T | missense_variant | MODERATE | c.4222G>A|p.Asp1408Asn |
S100 |
7 | BAA04g06880 | A04 | 4552006 | C | T | synonymous_variant | LOW | c.4191G>A|p.Glu1397Glu |
S192 |
8 | BAA04g06880 | A04 | 4552137 | C | T | missense_variant | MODERATE | c.4060G>A|p.Val1354Ile |
S178 |
9 | BAA04g06880 | A04 | 4552141 | C | T | synonymous_variant | LOW | c.4056G>A|p.Ser1352Ser |
S64 |
10 | BAA04g06880 | A04 | 4552405 | G | A | synonymous_variant | LOW | c.3792C>T|p.Val1264Val |
S259 S59 |
11 | BAA04g06880 | A04 | 4553763 | C | T | intron_variant | MODIFIER | c.3071-637G>A| |
S225 S73 |
12 | BAA04g06880 | A04 | 4553991 | G | A | intron_variant | MODIFIER | c.3070+657C>T| |
S303 |
13 | BAA04g06880 | A04 | 4554528 | G | A | intron_variant | MODIFIER | c.3070+120C>T| |
S160 |
14 | BAA04g06880 | A04 | 4554840 | C | T | missense_variant | MODERATE | c.2878G>A|p.Glu960Lys |
S247 |
15 | BAA04g06880 | A04 | 4554907 | G | A | synonymous_variant | LOW | c.2811C>T|p.Phe937Phe |
S13 |
16 | BAA04g06880 | A04 | 4554981 | C | T | missense_variant | MODERATE | c.2737G>A|p.Glu913Lys |
S249 |
17 | BAA04g06880 | A04 | 4555124 | G | A | missense_variant | MODERATE | c.2594C>T|p.Ser865Phe |
S126 |
18 | BAA04g06880 | A04 | 4555902 | G | A | intron_variant | MODIFIER | c.2041+128C>T| |
S208 S219 |
19 | BAA04g06880 | A04 | 4556679 | C | T | synonymous_variant | LOW | c.1392G>A|p.Glu464Glu |
S302 |
20 | BAA04g06880 | A04 | 4556743 | G | A | missense_variant | MODERATE | c.1328C>T|p.Ser443Phe |
S219 |
21 | BAA04g06880 | A04 | 4557045 | G | A | synonymous_variant | LOW | c.1026C>T|p.Pro342Pro |
S229 |
22 | BAA04g06880 | A04 | 4557216 | C | T | synonymous_variant | LOW | c.855G>A|p.Gly285Gly |
S297 |
23 | BAA04g06880 | A04 | 4559890 | G | A | upstream_gene_variant | MODIFIER | c.-445C>T| |
S59 |
24 | BAA04g06880 | A04 | 4560122 | G | A | upstream_gene_variant | MODIFIER | c.-677C>T| |
S62 |
25 | BAA04g06880 | A04 | 4563758 | G | A | upstream_gene_variant | MODIFIER | c.-4313C>T| |
S162 |