Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03460 | A01 | 1566571 | C | T | missense_variant | MODERATE | c.118G>A|p.Asp40Asn |
S260 |
2 | BAA01g03460 | A01 | 1566807 | G | A | synonymous_variant | LOW | c.78C>T|p.Asp26Asp |
S178 |
3 | BAA01g03460 | A01 | 1567684 | C | T | upstream_gene_variant | MODIFIER | c.-800G>A| |
S71 |
4 | BAA01g03460 | A01 | 1567911 | C | T | upstream_gene_variant | MODIFIER | c.-1027G>A| |
S166 |
5 | BAA01g03460 | A01 | 1568420 | G | A | upstream_gene_variant | MODIFIER | c.-1536C>T| |
S180 |
6 | BAA01g03460 | A01 | 1569002 | G | A | upstream_gene_variant | MODIFIER | c.-2118C>T| |
S103 |
7 | BAA01g03460 | A01 | 1569608 | G | A | upstream_gene_variant | MODIFIER | c.-2724C>T| |
S187 |
8 | BAA01g03460 | A01 | 1569617 | C | T | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S192 |
9 | BAA01g03460 | A01 | 1569765 | G | A | upstream_gene_variant | MODIFIER | c.-2881C>T| |
S262 |
10 | BAA01g03460 | A01 | 1569893 | G | A | upstream_gene_variant | MODIFIER | c.-3009C>T| |
S65 |
11 | BAA01g03460 | A01 | 1570355 | G | A | upstream_gene_variant | MODIFIER | c.-3471C>T| |
S202 |
12 | BAA01g03460 | A01 | 1571030 | C | T | upstream_gene_variant | MODIFIER | c.-4146G>A| |
S128 |