Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g25490 | A09 | 16437751 | G | A | missense_variant | MODERATE | c.193C>T|p.Pro65Ser |
S98 |
2 | BAA09g25490 | A09 | 16438155 | G | A | intron_variant | MODIFIER | c.185+256C>T| |
S53 |
3 | BAA09g25490 | A09 | 16438375 | G | A | intron_variant | MODIFIER | c.185+36C>T| |
S88 |
4 | BAA09g25490 | A09 | 16438423 | C | T | missense_variant | MODERATE | c.173G>A|p.Gly58Asp |
S279 |
5 | BAA09g25490 | A09 | 16438656 | C | T | missense_variant | MODERATE | c.28G>A|p.Gly10Ser |
S92 |
6 | BAA09g25490 | A09 | 16438676 | C | T | missense_variant | MODERATE | c.8G>A|p.Ser3Asn |
S176 |
7 | BAA09g25490 | A09 | 16440486 | C | T | upstream_gene_variant | MODIFIER | c.-1803G>A| |
S278 |
8 | BAA09g25490 | A09 | 16440842 | C | T | upstream_gene_variant | MODIFIER | c.-2159G>A| |
S207 |
9 | BAA09g25490 | A09 | 16442356 | C | T | upstream_gene_variant | MODIFIER | c.-3673G>A| |
S132 S137 S89 |
10 | BAA09g25490 | A09 | 16443271 | G | A | upstream_gene_variant | MODIFIER | c.-4588C>T| |
S152 |
11 | BAA09g25490 | A09 | 16443356 | C | T | upstream_gene_variant | MODIFIER | c.-4673G>A| |
S76 |
12 | BAA09g25490 | A09 | 16443401 | G | A | upstream_gene_variant | MODIFIER | c.-4718C>T| |
S244 |