Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13070 | A01 | 6201166 | G | A | upstream_gene_variant | MODIFIER | c.-2812G>A| |
S75 |
2 | BAA01g13070 | A01 | 6201746 | G | A | upstream_gene_variant | MODIFIER | c.-2232G>A| |
S142 |
3 | BAA01g13070 | A01 | 6202362 | C | T | upstream_gene_variant | MODIFIER | c.-1616C>T| |
S16 S217 S248 |
4 | BAA01g13070 | A01 | 6203501 | G | A | upstream_gene_variant | MODIFIER | c.-477G>A| |
S59 |
5 | BAA01g13070 | A01 | 6204030 | C | T | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S230 |
6 | BAA01g13070 | A01 | 6204328 | C | T | synonymous_variant | LOW | c.351C>T|p.Val117Val |
S161 |
7 | BAA01g13070 | A01 | 6204950 | C | T | missense_variant | MODERATE | c.635C>T|p.Ser212Phe |
S239 S33 |
8 | BAA01g13070 | A01 | 6205180 | C | T | missense_variant | MODERATE | c.865C>T|p.Pro289Ser |
S171 |
9 | BAA01g13070 | A01 | 6205416 | G | A | splice_region_variant&intron_variant | LOW | c.1096+5G>A| |
S271 |
10 | BAA01g13070 | A01 | 6205442 | C | T | intron_variant | MODIFIER | c.1096+31C>T| |
S81 S85 |
11 | BAA01g13070 | A01 | 6206288 | C | T | downstream_gene_variant | MODIFIER | c.*696C>T| |
S196 |
12 | BAA01g13070 | A01 | 6206311 | G | A | downstream_gene_variant | MODIFIER | c.*719G>A| |
S60 |
13 | BAA01g13070 | A01 | 6206673 | G | A | downstream_gene_variant | MODIFIER | c.*1081G>A| |
S110 S114 S125 S20 S202 S221 S23 S286 S289 S299 S46 S84 S99 |
14 | BAA01g13070 | A01 | 6208869 | G | A | downstream_gene_variant | MODIFIER | c.*3277G>A| |
S12 |
15 | BAA01g13070 | A01 | 6208945 | G | A | downstream_gene_variant | MODIFIER | c.*3353G>A| |
S129 |
16 | BAA01g13070 | A01 | 6208984 | G | A | downstream_gene_variant | MODIFIER | c.*3392G>A| |
S197 |
17 | BAA01g13070 | A01 | 6209379 | C | T | downstream_gene_variant | MODIFIER | c.*3787C>T| |
S44 |
18 | BAA01g13070 | A01 | 6210119 | C | T | downstream_gene_variant | MODIFIER | c.*4527C>T| |
S58 |