Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14590 | A09 | 8312503 | G | A | missense_variant | MODERATE | c.1255C>T|p.Pro419Ser |
S163 |
2 | BAA09g14590 | A09 | 8312532 | C | T | missense_variant | MODERATE | c.1226G>A|p.Arg409Gln |
S6 |
3 | BAA09g14590 | A09 | 8312594 | G | A | synonymous_variant | LOW | c.1164C>T|p.Ala388Ala |
S124 |
4 | BAA09g14590 | A09 | 8312620 | C | T | missense_variant | MODERATE | c.1138G>A|p.Ala380Thr |
S177 |
5 | BAA09g14590 | A09 | 8312644 | G | A | missense_variant | MODERATE | c.1114C>T|p.Arg372Trp |
S149 |
6 | BAA09g14590 | A09 | 8312715 | C | T | missense_variant | MODERATE | c.1043G>A|p.Gly348Glu |
S305 |
7 | BAA09g14590 | A09 | 8313467 | C | T | synonymous_variant | LOW | c.408G>A|p.Gly136Gly |
S293 |
8 | BAA09g14590 | A09 | 8313955 | C | T | upstream_gene_variant | MODIFIER | c.-81G>A| |
S212 |
9 | BAA09g14590 | A09 | 8314047 | G | A | upstream_gene_variant | MODIFIER | c.-173C>T| |
S202 |
10 | BAA09g14590 | A09 | 8315200 | C | T | upstream_gene_variant | MODIFIER | c.-1326G>A| |
S33 |
11 | BAA09g14590 | A09 | 8317025 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S23 |
12 | BAA09g14590 | A09 | 8317139 | C | T | upstream_gene_variant | MODIFIER | c.-3265G>A| |
S143 |
13 | BAA09g14590 | A09 | 8317258 | C | T | upstream_gene_variant | MODIFIER | c.-3384G>A| |
S302 |