Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20250 | A09 | 12490191 | C | T | downstream_gene_variant | MODIFIER | c.*4162G>A| |
S156 |
2 | BAA09g20250 | A09 | 12494373 | C | T | missense_variant | MODERATE | c.2590G>A|p.Glu864Lys |
S272 |
3 | BAA09g20250 | A09 | 12494549 | G | A | missense_variant | MODERATE | c.2414C>T|p.Pro805Leu |
S244 |
4 | BAA09g20250 | A09 | 12495497 | C | T | missense_variant | MODERATE | c.1466G>A|p.Gly489Glu |
S303 |
5 | BAA09g20250 | A09 | 12495521 | C | T | missense_variant | MODERATE | c.1442G>A|p.Gly481Asp |
S18 |
6 | BAA09g20250 | A09 | 12495586 | G | A | synonymous_variant | LOW | c.1377C>T|p.Leu459Leu |
S56 |
7 | BAA09g20250 | A09 | 12495651 | G | A | missense_variant | MODERATE | c.1312C>T|p.Pro438Ser |
S192 |
8 | BAA09g20250 | A09 | 12495969 | G | A | missense_variant | MODERATE | c.994C>T|p.Pro332Ser |
S221 |
9 | BAA09g20250 | A09 | 12496351 | C | T | stop_gained | HIGH | c.612G>A|p.Trp204* |
S287 |
10 | BAA09g20250 | A09 | 12496875 | G | A | missense_variant | MODERATE | c.88C>T|p.Pro30Ser |
S221 |
11 | BAA09g20250 | A09 | 12496955 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Leu |
S20 |
12 | BAA09g20250 | A09 | 12497212 | C | T | upstream_gene_variant | MODIFIER | c.-250G>A| |
S192 |
13 | BAA09g20250 | A09 | 12497450 | C | T | upstream_gene_variant | MODIFIER | c.-488G>A| |
S204 |
14 | BAA09g20250 | A09 | 12500505 | G | A | upstream_gene_variant | MODIFIER | c.-3543C>T| |
S286 |
15 | BAA09g20250 | A09 | 12500913 | C | T | upstream_gene_variant | MODIFIER | c.-3951G>A| |
S140 |