Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g49790 | A03 | 24002950 | G | A | synonymous_variant | LOW | c.4122C>T|p.Val1374Val |
S152 |
2 | BAA03g49790 | A03 | 24002986 | G | A | synonymous_variant | LOW | c.4086C>T|p.His1362His |
S112 |
3 | BAA03g49790 | A03 | 24003975 | C | T | missense_variant | MODERATE | c.3380G>A|p.Gly1127Glu |
S205 |
4 | BAA03g49790 | A03 | 24004349 | G | A | missense_variant | MODERATE | c.3164C>T|p.Ser1055Leu |
S210 S225 |
5 | BAA03g49790 | A03 | 24004391 | C | T | missense_variant | MODERATE | c.3122G>A|p.Arg1041Lys |
S249 S96 |
6 | BAA03g49790 | A03 | 24008478 | G | A | missense_variant | MODERATE | c.685C>T|p.Pro229Ser |
S247 |
7 | BAA03g49790 | A03 | 24008574 | G | A | synonymous_variant | LOW | c.589C>T|p.Leu197Leu |
S77 S82 |
8 | BAA03g49790 | A03 | 24008892 | C | T | missense_variant | MODERATE | c.433G>A|p.Glu145Lys |
S53 |
9 | BAA03g49790 | A03 | 24009617 | C | T | missense_variant | MODERATE | c.40G>A|p.Asp14Asn |
S211 S227 |
10 | BAA03g49790 | A03 | 24011174 | C | T | upstream_gene_variant | MODIFIER | c.-1425G>A| |
S251 |
11 | BAA03g49790 | A03 | 24011234 | G | A | upstream_gene_variant | MODIFIER | c.-1485C>T| |
S133 |
12 | BAA03g49790 | A03 | 24011726 | G | A | upstream_gene_variant | MODIFIER | c.-1977C>T| |
S7 |
13 | BAA03g49790 | A03 | 24012156 | C | T | upstream_gene_variant | MODIFIER | c.-2407G>A| |
S158 |
14 | BAA03g49790 | A03 | 24012788 | C | T | upstream_gene_variant | MODIFIER | c.-3039G>A| |
S67 |
15 | BAA03g49790 | A03 | 24013093 | G | A | upstream_gene_variant | MODIFIER | c.-3344C>T| |
S4 |
16 | BAA03g49790 | A03 | 24013158 | C | T | upstream_gene_variant | MODIFIER | c.-3409G>A| |
S299 |
17 | BAA03g49790 | A03 | 24013691 | C | G | upstream_gene_variant | MODIFIER | c.-3942G>C| |
S1 S90 |
18 | BAA03g49790 | A03 | 24013707 | A | T | upstream_gene_variant | MODIFIER | c.-3958T>A| |
S26 |
19 | BAA03g49790 | A03 | 24014011 | G | A | upstream_gene_variant | MODIFIER | c.-4262C>T| |
S128 |
20 | BAA03g49790 | A03 | 24014014 | C | T | upstream_gene_variant | MODIFIER | c.-4265G>A| |
S206 S26 |