Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g25160 | A01 | 13502202 | C | T | missense_variant | MODERATE | c.1103G>A|p.Gly368Glu |
S261 |
2 | BAA01g25160 | A01 | 13502237 | G | A | synonymous_variant | LOW | c.1068C>T|p.Phe356Phe |
S239 |
3 | BAA01g25160 | A01 | 13502402 | G | A | splice_region_variant&intron_variant | LOW | c.1014+8C>T| |
S84 S93 |
4 | BAA01g25160 | A01 | 13502409 | C | T | splice_donor_variant&intron_variant | HIGH | c.1014+1G>A| |
S255 |
5 | BAA01g25160 | A01 | 13502514 | G | A | intron_variant | MODIFIER | c.919-9C>T| |
S232 |
6 | BAA01g25160 | A01 | 13503245 | G | A | missense_variant | MODERATE | c.509C>T|p.Ser170Phe |
S279 |
7 | BAA01g25160 | A01 | 13503778 | G | A | missense_variant | MODERATE | c.320C>T|p.Ser107Phe |
S23 |
8 | BAA01g25160 | A01 | 13504091 | C | T | intron_variant | MODIFIER | c.129+41G>A| |
S4 |
9 | BAA01g25160 | A01 | 13504183 | G | A | synonymous_variant | LOW | c.78C>T|p.Leu26Leu |
S80 |
10 | BAA01g25160 | A01 | 13505151 | C | T | upstream_gene_variant | MODIFIER | c.-891G>A| |
S200 |
11 | BAA01g25160 | A01 | 13506688 | A | G | upstream_gene_variant | MODIFIER | c.-2428T>C| |
S210 |
12 | BAA01g25160 | A01 | 13508199 | G | A | upstream_gene_variant | MODIFIER | c.-3939C>T| |
S142 S251 |
13 | BAA01g25160 | A01 | 13508218 | G | A | upstream_gene_variant | MODIFIER | c.-3958C>T| |
S301 S304 |