Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36990 | A01 | 24714658 | G | A | upstream_gene_variant | MODIFIER | c.-4075G>A| |
S262 |
2 | BAA01g36990 | A01 | 24718936 | C | T | synonymous_variant | LOW | c.204C>T|p.Asp68Asp |
S98 |
3 | BAA01g36990 | A01 | 24718956 | G | A | missense_variant | MODERATE | c.224G>A|p.Gly75Asp |
S229 |
4 | BAA01g36990 | A01 | 24719593 | G | A | synonymous_variant | LOW | c.861G>A|p.Ala287Ala |
S223 |
5 | BAA01g36990 | A01 | 24719724 | G | A | intron_variant | MODIFIER | c.938+54G>A| |
S175 |
6 | BAA01g36990 | A01 | 24720570 | C | T | intron_variant | MODIFIER | c.938+900C>T| |
S192 |
7 | BAA01g36990 | A01 | 24722777 | G | A | intron_variant | MODIFIER | c.939-134G>A| |
S152 |
8 | BAA01g36990 | A01 | 24723390 | G | A | intron_variant | MODIFIER | c.1082+336G>A| |
S246 |
9 | BAA01g36990 | A01 | 24723527 | G | A | intron_variant | MODIFIER | c.1082+473G>A| |
S281 |
10 | BAA01g36990 | A01 | 24725240 | C | T | intron_variant | MODIFIER | c.1381-82C>T| |
S133 |
11 | BAA01g36990 | A01 | 24725437 | G | A | missense_variant | MODERATE | c.1496G>A|p.Gly499Glu |
S293 |
12 | BAA01g36990 | A01 | 24725496 | G | A | missense_variant | MODERATE | c.1555G>A|p.Val519Ile |
S157 S163 |
13 | BAA01g36990 | A01 | 24726138 | G | A | downstream_gene_variant | MODIFIER | c.*625G>A| |
S121 |
14 | BAA01g36990 | A01 | 24726707 | G | A | downstream_gene_variant | MODIFIER | c.*1194G>A| |
S257 |
15 | BAA01g36990 | A01 | 24729944 | C | T | downstream_gene_variant | MODIFIER | c.*4431C>T| |
S211 |