Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00580 | A08 | 393299 | C | T | upstream_gene_variant | MODIFIER | c.-4431C>T| |
S303 |
2 | BAA08g00580 | A08 | 397058 | C | T | upstream_gene_variant | MODIFIER | c.-672C>T| |
S233 |
3 | BAA08g00580 | A08 | 397396 | C | T | upstream_gene_variant | MODIFIER | c.-334C>T| |
S39 |
4 | BAA08g00580 | A08 | 397614 | C | T | upstream_gene_variant | MODIFIER | c.-116C>T| |
S113 |
5 | BAA08g00580 | A08 | 397891 | C | T | splice_region_variant&synonymous_variant | LOW | c.162C>T|p.Phe54Phe |
S135 |
6 | BAA08g00580 | A08 | 398551 | G | A | missense_variant | MODERATE | c.508G>A|p.Ala170Thr |
S249 |
7 | BAA08g00580 | A08 | 398774 | G | A | missense_variant | MODERATE | c.731G>A|p.Ser244Asn |
S20 |
8 | BAA08g00580 | A08 | 399638 | G | A | missense_variant | MODERATE | c.1243G>A|p.Asp415Asn |
S109 |
9 | BAA08g00580 | A08 | 400803 | G | A | synonymous_variant | LOW | c.2259G>A|p.Arg753Arg |
S85 |
10 | BAA08g00580 | A08 | 402077 | G | A | stop_gained&splice_region_variant | HIGH | c.2871G>A|p.Trp957* |
S202 |
11 | BAA08g00580 | A08 | 406024 | C | T | downstream_gene_variant | MODIFIER | c.*2891C>T| |
S251 |
12 | BAA08g00580 | A08 | 406110 | G | A | downstream_gene_variant | MODIFIER | c.*2977G>A| |
S192 |
13 | BAA08g00580 | A08 | 406607 | C | T | downstream_gene_variant | MODIFIER | c.*3474C>T| |
S114 |
14 | BAA08g00580 | A08 | 406924 | G | A | downstream_gene_variant | MODIFIER | c.*3791G>A| |
S217 S248 |
15 | BAA08g00580 | A08 | 407362 | C | T | downstream_gene_variant | MODIFIER | c.*4229C>T| |
S164 |
16 | BAA08g00580 | A08 | 407389 | C | T | downstream_gene_variant | MODIFIER | c.*4256C>T| |
S172 S217 |
17 | BAA08g00580 | A08 | 407785 | G | A | downstream_gene_variant | MODIFIER | c.*4652G>A| |
S119 |