Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29850 | A08 | 20383656 | G | A | missense_variant | MODERATE | c.1382C>T|p.Pro461Leu |
S232 |
2 | BAA08g29850 | A08 | 20384010 | C | T | synonymous_variant | LOW | c.1200G>A|p.Gln400Gln |
S200 S261 S303 |
3 | BAA08g29850 | A08 | 20384107 | C | T | missense_variant | MODERATE | c.1103G>A|p.Arg368Lys |
S206 S26 |
4 | BAA08g29850 | A08 | 20384130 | C | T | splice_region_variant&synonymous_variant | LOW | c.1080G>A|p.Gly360Gly |
S244 |
5 | BAA08g29850 | A08 | 20385035 | C | T | synonymous_variant | LOW | c.537G>A|p.Lys179Lys |
S148 S210 |
6 | BAA08g29850 | A08 | 20385151 | C | T | missense_variant | MODERATE | c.496G>A|p.Gly166Arg |
S28 |
7 | BAA08g29850 | A08 | 20385163 | C | T | missense_variant | MODERATE | c.484G>A|p.Asp162Asn |
S144 |
8 | BAA08g29850 | A08 | 20385166 | G | A | synonymous_variant | LOW | c.481C>T|p.Leu161Leu |
S229 |
9 | BAA08g29850 | A08 | 20385560 | C | T | missense_variant&splice_region_variant | MODERATE | c.319G>A|p.Glu107Lys |
S270 |
10 | BAA08g29850 | A08 | 20386756 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S19 |
11 | BAA08g29850 | A08 | 20387389 | G | A | upstream_gene_variant | MODIFIER | c.-1080C>T| |
S115 |
12 | BAA08g29850 | A08 | 20387408 | C | T | upstream_gene_variant | MODIFIER | c.-1099G>A| |
S4 |