Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g19770 | A07 | 25308065 | G | A | missense_variant&splice_region_variant | MODERATE | c.2167C>T|p.Pro723Ser |
S94 |
2 | BAA07g19770 | A07 | 25308553 | G | A | synonymous_variant | LOW | c.1848C>T|p.Ser616Ser |
S45 |
3 | BAA07g19770 | A07 | 25308593 | G | A | missense_variant | MODERATE | c.1808C>T|p.Ser603Phe |
S298 |
4 | BAA07g19770 | A07 | 25309054 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1450-1G>A| |
S211 S227 |
5 | BAA07g19770 | A07 | 25309089 | C | T | intron_variant | MODIFIER | c.1450-36G>A| |
S265 |
6 | BAA07g19770 | A07 | 25309339 | G | A | intron_variant | MODIFIER | c.1306-38C>T| |
S107 |
7 | BAA07g19770 | A07 | 25310364 | G | A | missense_variant | MODERATE | c.830C>T|p.Pro277Leu |
S235 |
8 | BAA07g19770 | A07 | 25310873 | G | A | missense_variant | MODERATE | c.550C>T|p.Leu184Phe |
S54 |
9 | BAA07g19770 | A07 | 25310920 | G | A | intron_variant | MODIFIER | c.520-17C>T| |
S67 |
10 | BAA07g19770 | A07 | 25311013 | G | A | splice_region_variant&intron_variant | LOW | c.519+8C>T| |
S255 |
11 | BAA07g19770 | A07 | 25312536 | G | A | upstream_gene_variant | MODIFIER | c.-789C>T| |
S296 |
12 | BAA07g19770 | A07 | 25313433 | G | A | upstream_gene_variant | MODIFIER | c.-1686C>T| |
S89 |
13 | BAA07g19770 | A07 | 25316412 | G | A | upstream_gene_variant | MODIFIER | c.-4665C>T| |
S106 |