Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21040 | A01 | 10353899 | G | A | missense_variant | MODERATE | c.1205C>T|p.Ser402Phe |
S152 |
2 | BAA01g21040 | A01 | 10354680 | G | A | missense_variant | MODERATE | c.424C>T|p.Pro142Ser |
S291 |
3 | BAA01g21040 | A01 | 10354764 | C | T | missense_variant | MODERATE | c.340G>A|p.Asp114Asn |
S99 |
4 | BAA01g21040 | A01 | 10355398 | C | T | upstream_gene_variant | MODIFIER | c.-295G>A| |
S9 |
5 | BAA01g21040 | A01 | 10355414 | G | A | upstream_gene_variant | MODIFIER | c.-311C>T| |
S108 |
6 | BAA01g21040 | A01 | 10355813 | C | T | upstream_gene_variant | MODIFIER | c.-710G>A| |
S303 |
7 | BAA01g21040 | A01 | 10356128 | C | T | upstream_gene_variant | MODIFIER | c.-1025G>A| |
S259 |
8 | BAA01g21040 | A01 | 10356255 | G | A | upstream_gene_variant | MODIFIER | c.-1152C>T| |
S70 |
9 | BAA01g21040 | A01 | 10356383 | G | A | upstream_gene_variant | MODIFIER | c.-1280C>T| |
S245 |
10 | BAA01g21040 | A01 | 10356657 | G | A | upstream_gene_variant | MODIFIER | c.-1554C>T| |
S123 |
11 | BAA01g21040 | A01 | 10357578 | C | T | upstream_gene_variant | MODIFIER | c.-2475G>A| |
S11 |
12 | BAA01g21040 | A01 | 10357579 | G | A | upstream_gene_variant | MODIFIER | c.-2476C>T| |
S293 |
13 | BAA01g21040 | A01 | 10357882 | C | T | upstream_gene_variant | MODIFIER | c.-2779G>A| |
S143 |
14 | BAA01g21040 | A01 | 10358192 | G | A | upstream_gene_variant | MODIFIER | c.-3089C>T| |
S7 |
15 | BAA01g21040 | A01 | 10359185 | C | T | upstream_gene_variant | MODIFIER | c.-4082G>A| |
S46 |
16 | BAA01g21040 | A01 | 10359943 | G | A | upstream_gene_variant | MODIFIER | c.-4840C>T| |
S239 |