Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19090 | A06 | 9814321 | C | T | downstream_gene_variant | MODIFIER | c.*3300G>A| |
S113 S120 S266 S9 |
2 | BAA06g19090 | A06 | 9814446 | C | T | downstream_gene_variant | MODIFIER | c.*3175G>A| |
S40 S49 |
3 | BAA06g19090 | A06 | 9815098 | C | G | downstream_gene_variant | MODIFIER | c.*2523G>C| |
S38 |
4 | BAA06g19090 | A06 | 9815461 | C | T | downstream_gene_variant | MODIFIER | c.*2160G>A| |
S301 S304 |
5 | BAA06g19090 | A06 | 9815805 | G | A | downstream_gene_variant | MODIFIER | c.*1816C>T| |
S152 |
6 | BAA06g19090 | A06 | 9816565 | C | T | downstream_gene_variant | MODIFIER | c.*1056G>A| |
S159 S243 |
7 | BAA06g19090 | A06 | 9817401 | G | A | downstream_gene_variant | MODIFIER | c.*220C>T| |
S71 |
8 | BAA06g19090 | A06 | 9818068 | C | T | missense_variant | MODERATE | c.659G>A|p.Arg220His |
S15 S3 |
9 | BAA06g19090 | A06 | 9818243 | G | A | missense_variant | MODERATE | c.566C>T|p.Pro189Leu |
S122 |
10 | BAA06g19090 | A06 | 9818278 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.532-1G>A| |
S186 |
11 | BAA06g19090 | A06 | 9819700 | G | A | upstream_gene_variant | MODIFIER | c.-289C>T| |
S95 |
12 | BAA06g19090 | A06 | 9820011 | C | T | upstream_gene_variant | MODIFIER | c.-600G>A| |
S84 S93 |
13 | BAA06g19090 | A06 | 9820570 | G | A | upstream_gene_variant | MODIFIER | c.-1159C>T| |
S230 |