Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g54770 | A03 | 27028940 | C | T | missense_variant | MODERATE | c.2296G>A|p.Val766Ile |
S6 |
2 | BAA03g54770 | A03 | 27028946 | C | T | missense_variant | MODERATE | c.2290G>A|p.Val764Ile |
S263 |
3 | BAA03g54770 | A03 | 27029502 | C | T | synonymous_variant | LOW | c.1734G>A|p.Lys578Lys |
S94 |
4 | BAA03g54770 | A03 | 27029579 | C | T | missense_variant | MODERATE | c.1657G>A|p.Glu553Lys |
S280 |
5 | BAA03g54770 | A03 | 27030080 | C | T | missense_variant | MODERATE | c.1360G>A|p.Glu454Lys |
S139 |
6 | BAA03g54770 | A03 | 27030832 | G | A | missense_variant | MODERATE | c.985C>T|p.Pro329Ser |
S212 |
7 | BAA03g54770 | A03 | 27031137 | G | A | missense_variant | MODERATE | c.901C>T|p.Leu301Phe |
S239 |
8 | BAA03g54770 | A03 | 27031454 | C | T | splice_region_variant&intron_variant | LOW | c.734+5G>A| |
S142 |
9 | BAA03g54770 | A03 | 27031672 | C | T | synonymous_variant | LOW | c.606G>A|p.Lys202Lys |
S165 |
10 | BAA03g54770 | A03 | 27032071 | G | A | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S217 S248 |
11 | BAA03g54770 | A03 | 27032273 | G | A | synonymous_variant | LOW | c.165C>T|p.Pro55Pro |
S84 S93 |
12 | BAA03g54770 | A03 | 27032352 | G | A | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S275 |
13 | BAA03g54770 | A03 | 27033132 | G | A | upstream_gene_variant | MODIFIER | c.-695C>T| |
S153 S213 |
14 | BAA03g54770 | A03 | 27033310 | C | A | upstream_gene_variant | MODIFIER | c.-873G>T| |
S25 |
15 | BAA03g54770 | A03 | 27034004 | G | A | upstream_gene_variant | MODIFIER | c.-1567C>T| |
S297 |
16 | BAA03g54770 | A03 | 27034392 | C | T | upstream_gene_variant | MODIFIER | c.-1955G>A| |
S165 |
17 | BAA03g54770 | A03 | 27036349 | G | A | upstream_gene_variant | MODIFIER | c.-3912C>T| |
S221 |