Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00820 | A06 | 588803 | G | A | upstream_gene_variant | MODIFIER | c.-3257G>A| |
S169 |
2 | BAA06g00820 | A06 | 592386 | C | T | missense_variant | MODERATE | c.236C>T|p.Ala79Val |
S25 |
3 | BAA06g00820 | A06 | 592832 | G | A | synonymous_variant | LOW | c.501G>A|p.Leu167Leu |
S143 |
4 | BAA06g00820 | A06 | 593504 | G | A | missense_variant&splice_region_variant | MODERATE | c.763G>A|p.Glu255Lys |
S172 S217 |
5 | BAA06g00820 | A06 | 593617 | G | A | synonymous_variant | LOW | c.792G>A|p.Lys264Lys |
S33 |
6 | BAA06g00820 | A06 | 593811 | G | A | stop_gained&splice_region_variant | HIGH | c.986G>A|p.Trp329* |
S244 |
7 | BAA06g00820 | A06 | 594541 | G | A | missense_variant | MODERATE | c.1340G>A|p.Arg447Lys |
S165 |
8 | BAA06g00820 | A06 | 594802 | C | T | missense_variant | MODERATE | c.1493C>T|p.Ser498Phe |
S167 |
9 | BAA06g00820 | A06 | 594895 | G | A | missense_variant&splice_region_variant | MODERATE | c.1586G>A|p.Gly529Glu |
S186 |