Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00500 | A08 | 326556 | T | A | upstream_gene_variant | MODIFIER | c.-3566T>A| |
S145 S194 S195 S209 S246 S66 |
2 | BAA08g00500 | A08 | 326985 | C | T | upstream_gene_variant | MODIFIER | c.-3137C>T| |
S17 |
3 | BAA08g00500 | A08 | 327085 | G | A | upstream_gene_variant | MODIFIER | c.-3037G>A| |
S8 |
4 | BAA08g00500 | A08 | 327535 | C | T | upstream_gene_variant | MODIFIER | c.-2587C>T| |
S60 |
5 | BAA08g00500 | A08 | 328502 | C | T | upstream_gene_variant | MODIFIER | c.-1620C>T| |
S164 |
6 | BAA08g00500 | A08 | 330365 | C | T | missense_variant | MODERATE | c.244C>T|p.Pro82Ser |
S140 |
7 | BAA08g00500 | A08 | 331311 | G | A | intron_variant | MODIFIER | c.506-293G>A| |
S306 |
8 | BAA08g00500 | A08 | 331541 | C | T | intron_variant | MODIFIER | c.506-63C>T| |
S6 |
9 | BAA08g00500 | A08 | 332002 | G | A | synonymous_variant | LOW | c.825G>A|p.Arg275Arg |
S20 |
10 | BAA08g00500 | A08 | 332059 | G | A | synonymous_variant | LOW | c.882G>A|p.Arg294Arg |
S181 |
11 | BAA08g00500 | A08 | 332164 | C | T | intron_variant | MODIFIER | c.911+76C>T| |
S168 |
12 | BAA08g00500 | A08 | 334220 | G | A | downstream_gene_variant | MODIFIER | c.*1524G>A| |
S282 |
13 | BAA08g00500 | A08 | 335793 | C | T | downstream_gene_variant | MODIFIER | c.*3097C>T| |
S7 |