Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g02170 | A05 | 1190897 | G | A | upstream_gene_variant | MODIFIER | c.-3794G>A| |
S257 |
2 | BAA05g02170 | A05 | 1191611 | G | T | upstream_gene_variant | MODIFIER | c.-3080G>T| |
S157 S163 |
3 | BAA05g02170 | A05 | 1191784 | G | A | upstream_gene_variant | MODIFIER | c.-2907G>A| |
S152 |
4 | BAA05g02170 | A05 | 1191851 | G | A | upstream_gene_variant | MODIFIER | c.-2840G>A| |
S76 |
5 | BAA05g02170 | A05 | 1194800 | A | G | missense_variant | MODERATE | c.110A>G|p.Asp37Gly |
S287 |
6 | BAA05g02170 | A05 | 1195136 | C | T | missense_variant | MODERATE | c.446C>T|p.Ser149Leu |
S92 |
7 | BAA05g02170 | A05 | 1195291 | C | T | missense_variant | MODERATE | c.601C>T|p.Pro201Ser |
S256 |
8 | BAA05g02170 | A05 | 1195501 | G | A | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S6 |
9 | BAA05g02170 | A05 | 1195543 | G | A | missense_variant | MODERATE | c.853G>A|p.Glu285Lys |
S79 S84 |
10 | BAA05g02170 | A05 | 1195647 | C | T | synonymous_variant | LOW | c.957C>T|p.Ala319Ala |
S20 |
11 | BAA05g02170 | A05 | 1195803 | G | A | synonymous_variant | LOW | c.1113G>A|p.Glu371Glu |
S209 |
12 | BAA05g02170 | A05 | 1195879 | C | T | missense_variant | MODERATE | c.1189C>T|p.Leu397Phe |
S183 S198 |
13 | BAA05g02170 | A05 | 1196197 | C | T | missense_variant | MODERATE | c.1507C>T|p.Pro503Ser |
S256 |
14 | BAA05g02170 | A05 | 1196369 | C | T | missense_variant | MODERATE | c.1679C>T|p.Thr560Ile |
S153 S213 |
15 | BAA05g02170 | A05 | 1196555 | C | T | missense_variant | MODERATE | c.1865C>T|p.Pro622Leu |
S297 |
16 | BAA05g02170 | A05 | 1198724 | C | T | downstream_gene_variant | MODIFIER | c.*2102C>T| |
S107 |
17 | BAA05g02170 | A05 | 1199098 | C | T | downstream_gene_variant | MODIFIER | c.*2476C>T| |
S235 |
18 | BAA05g02170 | A05 | 1200482 | G | A | downstream_gene_variant | MODIFIER | c.*3860G>A| |
S186 |
19 | BAA05g02170 | A05 | 1201093 | G | A | downstream_gene_variant | MODIFIER | c.*4471G>A| |
S191 |