Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g30960 | A10 | 22753909 | G | A | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S178 |
2 | BAA10g30960 | A10 | 22754754 | G | A | upstream_gene_variant | MODIFIER | c.-4059G>A| |
S50 |
3 | BAA10g30960 | A10 | 22755878 | C | T | upstream_gene_variant | MODIFIER | c.-2935C>T| |
S295 |
4 | BAA10g30960 | A10 | 22758048 | G | A | upstream_gene_variant | MODIFIER | c.-765G>A| |
S223 |
5 | BAA10g30960 | A10 | 22759164 | G | A | synonymous_variant | LOW | c.57G>A|p.Pro19Pro |
S18 S256 |
6 | BAA10g30960 | A10 | 22759366 | C | T | missense_variant | MODERATE | c.101C>T|p.Ser34Leu |
S168 |
7 | BAA10g30960 | A10 | 22759422 | C | T | missense_variant | MODERATE | c.157C>T|p.Pro53Ser |
S203 |
8 | BAA10g30960 | A10 | 22759703 | C | T | synonymous_variant | LOW | c.351C>T|p.Tyr117Tyr |
S308 |
9 | BAA10g30960 | A10 | 22760028 | G | A | intron_variant | MODIFIER | c.410-85G>A| |
S173 |
10 | BAA10g30960 | A10 | 22760085 | G | A | intron_variant | MODIFIER | c.410-28G>A| |
S46 |
11 | BAA10g30960 | A10 | 22760150 | G | A | stop_gained | HIGH | c.447G>A|p.Trp149* |
S71 |
12 | BAA10g30960 | A10 | 22761628 | C | T | missense_variant | MODERATE | c.1286C>T|p.Pro429Leu |
S112 |
13 | BAA10g30960 | A10 | 22761689 | G | A | intron_variant | MODIFIER | c.1328+19G>A| |
S174 |
14 | BAA10g30960 | A10 | 22763136 | A | C | missense_variant | MODERATE | c.1944A>C|p.Glu648Asp |
S110 S112 S121 S147 S163 S199 S219 S222 S240 S48 S70 S83 S93 |
15 | BAA10g30960 | A10 | 22763789 | C | T | missense_variant | MODERATE | c.2099C>T|p.Pro700Leu |
S89 |
16 | BAA10g30960 | A10 | 22766373 | G | A | synonymous_variant | LOW | c.3048G>A|p.Glu1016Glu |
S228 |
17 | BAA10g30960 | A10 | 22766956 | G | A | missense_variant | MODERATE | c.3331G>A|p.Val1111Met |
S139 |