Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g42090 | A07 | 36679965 | G | A | synonymous_variant | LOW | c.2019C>T|p.Pro673Pro |
S136 |
2 | BAA07g42090 | A07 | 36680199 | C | T | synonymous_variant | LOW | c.1785G>A|p.Arg595Arg |
S32 |
3 | BAA07g42090 | A07 | 36680200 | C | T | missense_variant | MODERATE | c.1784G>A|p.Arg595Lys |
S79 |
4 | BAA07g42090 | A07 | 36680358 | C | T | synonymous_variant | LOW | c.1695G>A|p.Lys565Lys |
S280 |
5 | BAA07g42090 | A07 | 36680489 | C | T | missense_variant | MODERATE | c.1634G>A|p.Gly545Glu |
S38 |
6 | BAA07g42090 | A07 | 36680574 | C | T | missense_variant | MODERATE | c.1549G>A|p.Glu517Lys |
S246 |
7 | BAA07g42090 | A07 | 36680653 | C | T | stop_gained | HIGH | c.1470G>A|p.Trp490* |
S165 |
8 | BAA07g42090 | A07 | 36681065 | G | A | missense_variant | MODERATE | c.1058C>T|p.Thr353Ile |
S245 |
9 | BAA07g42090 | A07 | 36681071 | G | A | missense_variant | MODERATE | c.1052C>T|p.Ala351Val |
S43 |
10 | BAA07g42090 | A07 | 36681441 | C | T | missense_variant | MODERATE | c.682G>A|p.Glu228Lys |
S20 |
11 | BAA07g42090 | A07 | 36681519 | C | T | missense_variant | MODERATE | c.604G>A|p.Gly202Arg |
S279 |
12 | BAA07g42090 | A07 | 36681537 | C | T | missense_variant | MODERATE | c.586G>A|p.Gly196Arg |
S117 |
13 | BAA07g42090 | A07 | 36681928 | C | T | synonymous_variant | LOW | c.195G>A|p.Glu65Glu |
S293 S35 |
14 | BAA07g42090 | A07 | 36682418 | C | T | upstream_gene_variant | MODIFIER | c.-296G>A| |
S58 |
15 | BAA07g42090 | A07 | 36682985 | G | A | upstream_gene_variant | MODIFIER | c.-863C>T| |
S75 S81 |
16 | BAA07g42090 | A07 | 36683657 | C | T | upstream_gene_variant | MODIFIER | c.-1535G>A| |
S161 |
17 | BAA07g42090 | A07 | 36685806 | G | A | upstream_gene_variant | MODIFIER | c.-3684C>T| |
S134 |
18 | BAA07g42090 | A07 | 36685930 | C | T | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S25 |