Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11530 | A10 | 13139011 | C | T | upstream_gene_variant | MODIFIER | c.-2314C>T| |
S79 S91 |
2 | BAA10g11530 | A10 | 13140418 | G | A | upstream_gene_variant | MODIFIER | c.-907G>A| |
S50 |
3 | BAA10g11530 | A10 | 13140708 | C | T | upstream_gene_variant | MODIFIER | c.-617C>T| |
S81 S85 |
4 | BAA10g11530 | A10 | 13140862 | C | T | upstream_gene_variant | MODIFIER | c.-463C>T| |
S230 |
5 | BAA10g11530 | A10 | 13141620 | G | A | missense_variant&splice_region_variant | MODERATE | c.296G>A|p.Arg99Gln |
S215 |
6 | BAA10g11530 | A10 | 13141709 | G | A | splice_region_variant&synonymous_variant | LOW | c.300G>A|p.Ala100Ala |
S261 |
7 | BAA10g11530 | A10 | 13143593 | G | A | synonymous_variant | LOW | c.1335G>A|p.Glu445Glu |
S105 S106 |
8 | BAA10g11530 | A10 | 13143625 | G | A | splice_region_variant&intron_variant | LOW | c.1362+5G>A| |
S75 S81 |
9 | BAA10g11530 | A10 | 13143859 | C | T | missense_variant | MODERATE | c.1502C>T|p.Ser501Phe |
S121 |
10 | BAA10g11530 | A10 | 13148577 | G | A | downstream_gene_variant | MODIFIER | c.*4219G>A| |
S286 |
11 | BAA10g11530 | A10 | 13148953 | C | T | downstream_gene_variant | MODIFIER | c.*4595C>T| |
S298 |