Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26610 | A10 | 21041803 | C | A | synonymous_variant | LOW | c.2679G>T|p.Leu893Leu |
S288 |
2 | BAA10g26610 | A10 | 21041811 | C | T | missense_variant | MODERATE | c.2671G>A|p.Val891Ile |
S13 |
3 | BAA10g26610 | A10 | 21042560 | C | T | missense_variant | MODERATE | c.2039G>A|p.Gly680Glu |
S209 |
4 | BAA10g26610 | A10 | 21042690 | C | A | missense_variant | MODERATE | c.1909G>T|p.Ala637Ser |
S12 S260 S91 |
5 | BAA10g26610 | A10 | 21043739 | G | A | missense_variant | MODERATE | c.860C>T|p.Ser287Leu |
S71 |
6 | BAA10g26610 | A10 | 21044007 | C | T | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S96 |
7 | BAA10g26610 | A10 | 21046834 | T | G | upstream_gene_variant | MODIFIER | c.-1620A>C| |
S148 S236 |
8 | BAA10g26610 | A10 | 21046914 | C | T | upstream_gene_variant | MODIFIER | c.-1700G>A| |
S210 |