Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g33860 | A01 | 22623572 | G | A | downstream_gene_variant | MODIFIER | c.*3989C>T| |
S119 S274 |
2 | BAA01g33860 | A01 | 22624278 | C | T | downstream_gene_variant | MODIFIER | c.*3283G>A| |
S107 |
3 | BAA01g33860 | A01 | 22624330 | G | A | downstream_gene_variant | MODIFIER | c.*3231C>T| |
S199 |
4 | BAA01g33860 | A01 | 22624522 | A | T | downstream_gene_variant | MODIFIER | c.*3039T>A| |
S99 |
5 | BAA01g33860 | A01 | 22626007 | C | T | downstream_gene_variant | MODIFIER | c.*1554G>A| |
S50 |
6 | BAA01g33860 | A01 | 22627043 | C | T | downstream_gene_variant | MODIFIER | c.*518G>A| |
S142 |
7 | BAA01g33860 | A01 | 22627173 | C | T | downstream_gene_variant | MODIFIER | c.*388G>A| |
S44 |
8 | BAA01g33860 | A01 | 22627446 | G | A | downstream_gene_variant | MODIFIER | c.*115C>T| |
S278 |
9 | BAA01g33860 | A01 | 22627755 | C | T | missense_variant&splice_region_variant | MODERATE | c.1414G>A|p.Val472Met |
S213 |
10 | BAA01g33860 | A01 | 22628092 | C | T | missense_variant | MODERATE | c.1306G>A|p.Val436Ile |
S193 |
11 | BAA01g33860 | A01 | 22628131 | C | T | missense_variant | MODERATE | c.1267G>A|p.Glu423Lys |
S150 |
12 | BAA01g33860 | A01 | 22628340 | C | T | missense_variant | MODERATE | c.1058G>A|p.Arg353Lys |
S19 |
13 | BAA01g33860 | A01 | 22628744 | C | T | synonymous_variant | LOW | c.654G>A|p.Leu218Leu |
S57 |
14 | BAA01g33860 | A01 | 22628905 | C | T | missense_variant | MODERATE | c.493G>A|p.Asp165Asn |
S64 |
15 | BAA01g33860 | A01 | 22628961 | G | A | missense_variant | MODERATE | c.437C>T|p.Ala146Val |
S292 |
16 | BAA01g33860 | A01 | 22630243 | C | T | upstream_gene_variant | MODIFIER | c.-846G>A| |
S120 |
17 | BAA01g33860 | A01 | 22630379 | C | T | upstream_gene_variant | MODIFIER | c.-982G>A| |
S64 |
18 | BAA01g33860 | A01 | 22630661 | C | T | upstream_gene_variant | MODIFIER | c.-1264G>A| |
S256 |
19 | BAA01g33860 | A01 | 22632710 | C | T | upstream_gene_variant | MODIFIER | c.-3313G>A| |
S256 |