Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19950 | A05 | 12140651 | G | A | synonymous_variant | LOW | c.1581C>T|p.Phe527Phe |
S120 |
2 | BAA05g19950 | A05 | 12140722 | C | T | missense_variant | MODERATE | c.1510G>A|p.Glu504Lys |
S97 |
3 | BAA05g19950 | A05 | 12140919 | G | A | missense_variant | MODERATE | c.1313C>T|p.Ala438Val |
S301 S304 |
4 | BAA05g19950 | A05 | 12141010 | C | T | missense_variant | MODERATE | c.1222G>A|p.Ala408Thr |
S113 |
5 | BAA05g19950 | A05 | 12141122 | G | A | synonymous_variant | LOW | c.1110C>T|p.Arg370Arg |
S276 |
6 | BAA05g19950 | A05 | 12141476 | G | A | synonymous_variant | LOW | c.843C>T|p.Leu281Leu |
S161 |
7 | BAA05g19950 | A05 | 12141759 | C | T | missense_variant | MODERATE | c.560G>A|p.Gly187Glu |
S122 |
8 | BAA05g19950 | A05 | 12142188 | G | A | missense_variant | MODERATE | c.131C>T|p.Ser44Phe |
S95 |
9 | BAA05g19950 | A05 | 12142201 | G | A | stop_gained | HIGH | c.118C>T|p.Gln40* |
S122 |
10 | BAA05g19950 | A05 | 12143968 | C | T | splice_region_variant&intron_variant | LOW | c.43+4G>A| |
S18 |
11 | BAA05g19950 | A05 | 12144006 | G | A | synonymous_variant | LOW | c.9C>T|p.Arg3Arg |
S172 |
12 | BAA05g19950 | A05 | 12144706 | G | A | upstream_gene_variant | MODIFIER | c.-692C>T| |
S238 |
13 | BAA05g19950 | A05 | 12145746 | T | G | upstream_gene_variant | MODIFIER | c.-1732A>C| |
S117 |
14 | BAA05g19950 | A05 | 12146696 | G | A | upstream_gene_variant | MODIFIER | c.-2682C>T| |
S282 |
15 | BAA05g19950 | A05 | 12147145 | G | A | upstream_gene_variant | MODIFIER | c.-3131C>T| |
S124 |
16 | BAA05g19950 | A05 | 12147299 | G | A | upstream_gene_variant | MODIFIER | c.-3285C>T| |
S219 S72 |
17 | BAA05g19950 | A05 | 12147316 | G | A | upstream_gene_variant | MODIFIER | c.-3302C>T| |
S11 |
18 | BAA05g19950 | A05 | 12148454 | G | A | upstream_gene_variant | MODIFIER | c.-4440C>T| |
S161 |