Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00070 | A01 | 27982 | G | A | missense_variant | MODERATE | c.133G>A|p.Gly45Ser |
S200 |
2 | BAA01g00070 | A01 | 28150 | G | A | missense_variant | MODERATE | c.301G>A|p.Asp101Asn |
S60 |
3 | BAA01g00070 | A01 | 29091 | G | A | missense_variant | MODERATE | c.1159G>A|p.Glu387Lys |
S194 |
4 | BAA01g00070 | A01 | 30068 | C | T | missense_variant | MODERATE | c.2026C>T|p.Pro676Ser |
S167 |
5 | BAA01g00070 | A01 | 30154 | G | A | synonymous_variant | LOW | c.2112G>A|p.Lys704Lys |
S294 |
6 | BAA01g00070 | A01 | 30172 | G | A | synonymous_variant | LOW | c.2130G>A|p.Glu710Glu |
S264 |
7 | BAA01g00070 | A01 | 31177 | C | T | synonymous_variant | LOW | c.3135C>T|p.Phe1045Phe |
S231 |
8 | BAA01g00070 | A01 | 31212 | C | T | missense_variant | MODERATE | c.3170C>T|p.Ala1057Val |
S81 S85 |
9 | BAA01g00070 | A01 | 31512 | G | A | downstream_gene_variant | MODIFIER | c.*137G>A| |
S82 S92 |
10 | BAA01g00070 | A01 | 32313 | G | A | downstream_gene_variant | MODIFIER | c.*938G>A| |
S60 |
11 | BAA01g00070 | A01 | 32427 | G | A | downstream_gene_variant | MODIFIER | c.*1052G>A| |
S295 |
12 | BAA01g00070 | A01 | 32611 | G | A | downstream_gene_variant | MODIFIER | c.*1236G>A| |
S126 |
13 | BAA01g00070 | A01 | 32727 | G | A | downstream_gene_variant | MODIFIER | c.*1352G>A| |
S186 |
14 | BAA01g00070 | A01 | 32846 | G | A | downstream_gene_variant | MODIFIER | c.*1471G>A| |
S13 |
15 | BAA01g00070 | A01 | 32965 | G | A | downstream_gene_variant | MODIFIER | c.*1590G>A| |
S15 S3 |
16 | BAA01g00070 | A01 | 33177 | G | A | downstream_gene_variant | MODIFIER | c.*1802G>A| |
S245 |
17 | BAA01g00070 | A01 | 33340 | G | A | downstream_gene_variant | MODIFIER | c.*1965G>A| |
S260 |
18 | BAA01g00070 | A01 | 33553 | C | T | downstream_gene_variant | MODIFIER | c.*2178C>T| |
S236 |