Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g32370 | A05 | 34565240 | C | T | upstream_gene_variant | MODIFIER | c.-4351C>T| |
S139 |
2 | BAA05g32370 | A05 | 34565390 | C | T | upstream_gene_variant | MODIFIER | c.-4201C>T| |
S204 |
3 | BAA05g32370 | A05 | 34565934 | C | T | upstream_gene_variant | MODIFIER | c.-3657C>T| |
S130 |
4 | BAA05g32370 | A05 | 34567347 | C | T | upstream_gene_variant | MODIFIER | c.-2244C>T| |
S99 |
5 | BAA05g32370 | A05 | 34567747 | G | A | upstream_gene_variant | MODIFIER | c.-1844G>A| |
S156 |
6 | BAA05g32370 | A05 | 34569118 | G | A | upstream_gene_variant | MODIFIER | c.-473G>A| |
S118 |
7 | BAA05g32370 | A05 | 34570325 | G | A | stop_gained | HIGH | c.735G>A|p.Trp245* |
S77 S82 |
8 | BAA05g32370 | A05 | 34570773 | C | T | missense_variant | MODERATE | c.1183C>T|p.Leu395Phe |
S12 |
9 | BAA05g32370 | A05 | 34570968 | C | T | missense_variant | MODERATE | c.1378C>T|p.Pro460Ser |
S295 |
10 | BAA05g32370 | A05 | 34571083 | G | A | missense_variant | MODERATE | c.1493G>A|p.Arg498Lys |
S169 |
11 | BAA05g32370 | A05 | 34571201 | G | A | synonymous_variant | LOW | c.1611G>A|p.Lys537Lys |
S56 |
12 | BAA05g32370 | A05 | 34571499 | C | T | synonymous_variant | LOW | c.1909C>T|p.Leu637Leu |
S160 |
13 | BAA05g32370 | A05 | 34571871 | C | T | synonymous_variant | LOW | c.2181C>T|p.Phe727Phe |
S137 S215 |
14 | BAA05g32370 | A05 | 34572159 | G | A | splice_region_variant&intron_variant | LOW | c.2246-6G>A| |
S20 |
15 | BAA05g32370 | A05 | 34572598 | G | A | missense_variant | MODERATE | c.2531G>A|p.Arg844Lys |
S176 |
16 | BAA05g32370 | A05 | 34573202 | G | A | missense_variant | MODERATE | c.2863G>A|p.Glu955Lys |
S128 |
17 | BAA05g32370 | A05 | 34573527 | G | A | missense_variant | MODERATE | c.3188G>A|p.Gly1063Glu |
S275 |
18 | BAA05g32370 | A05 | 34576038 | G | A | downstream_gene_variant | MODIFIER | c.*2354G>A| |
S186 |
19 | BAA05g32370 | A05 | 34576436 | G | A | downstream_gene_variant | MODIFIER | c.*2752G>A| |
S7 |