Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g67080 | A03 | 41575328 | G | A | intron_variant | MODIFIER | c.633+13G>A| |
S260 |
2 | BAA03g67080 | A03 | 41575522 | G | A | missense_variant | MODERATE | c.754G>A|p.Asp252Asn |
S136 |
3 | BAA03g67080 | A03 | 41575604 | G | A | missense_variant | MODERATE | c.836G>A|p.Cys279Tyr |
S182 |
4 | BAA03g67080 | A03 | 41576158 | G | A | missense_variant | MODERATE | c.1390G>A|p.Val464Met |
S136 |
5 | BAA03g67080 | A03 | 41576706 | G | A | intron_variant | MODIFIER | c.1567-112G>A| |
S167 |
6 | BAA03g67080 | A03 | 41577080 | G | A | missense_variant | MODERATE | c.1714G>A|p.Glu572Lys |
S128 |
7 | BAA03g67080 | A03 | 41577295 | C | T | synonymous_variant | LOW | c.1929C>T|p.Leu643Leu |
S244 |
8 | BAA03g67080 | A03 | 41577532 | G | A | synonymous_variant | LOW | c.2166G>A|p.Lys722Lys |
S241 |
9 | BAA03g67080 | A03 | 41577576 | C | T | missense_variant | MODERATE | c.2210C>T|p.Ala737Val |
S207 |
10 | BAA03g67080 | A03 | 41577704 | C | T | missense_variant | MODERATE | c.2338C>T|p.Pro780Ser |
S153 |
11 | BAA03g67080 | A03 | 41578302 | G | A | synonymous_variant | LOW | c.2694G>A|p.Leu898Leu |
S242 |
12 | BAA03g67080 | A03 | 41578932 | C | T | stop_gained | HIGH | c.3118C>T|p.Gln1040* |
S47 |
13 | BAA03g67080 | A03 | 41579061 | G | A | missense_variant | MODERATE | c.3247G>A|p.Gly1083Ser |
S36 |
14 | BAA03g67080 | A03 | 41579136 | C | T | synonymous_variant | LOW | c.3322C>T|p.Leu1108Leu |
S232 |
15 | BAA03g67080 | A03 | 41579911 | G | A | downstream_gene_variant | MODIFIER | c.*254G>A| |
S267 |