Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g38960 | A03 | 18070085 | C | T | synonymous_variant | LOW | c.3429G>A|p.Lys1143Lys |
S94 |
2 | BAA03g38960 | A03 | 18070311 | G | A | synonymous_variant | LOW | c.3276C>T|p.Thr1092Thr |
S5 |
3 | BAA03g38960 | A03 | 18070675 | C | T | missense_variant | MODERATE | c.2912G>A|p.Gly971Glu |
S156 |
4 | BAA03g38960 | A03 | 18071564 | G | A | intron_variant | MODIFIER | c.2729-706C>T| |
S184 |
5 | BAA03g38960 | A03 | 18072538 | C | T | intron_variant | MODIFIER | c.2728+15G>A| |
S153 |
6 | BAA03g38960 | A03 | 18073684 | C | T | missense_variant | MODERATE | c.2062G>A|p.Glu688Lys |
S221 |
7 | BAA03g38960 | A03 | 18073694 | G | A | splice_region_variant&synonymous_variant | LOW | c.2052C>T|p.Leu684Leu |
S231 |
8 | BAA03g38960 | A03 | 18073993 | G | A | missense_variant | MODERATE | c.1985C>T|p.Ala662Val |
S267 |
9 | BAA03g38960 | A03 | 18074083 | C | T | intron_variant | MODIFIER | c.1977+16G>A| |
S155 |
10 | BAA03g38960 | A03 | 18074147 | G | A | synonymous_variant | LOW | c.1929C>T|p.Asp643Asp |
S13 S140 S219 S279 S64 S72 |
11 | BAA03g38960 | A03 | 18074375 | C | T | intron_variant | MODIFIER | c.1862+116G>A| |
S239 |
12 | BAA03g38960 | A03 | 18075419 | C | T | stop_gained | HIGH | c.1359G>A|p.Trp453* |
S34 |
13 | BAA03g38960 | A03 | 18076527 | C | T | missense_variant | MODERATE | c.859G>A|p.Val287Met |
S187 |
14 | BAA03g38960 | A03 | 18076575 | G | A | intron_variant | MODIFIER | c.855-44C>T| |
S67 |
15 | BAA03g38960 | A03 | 18076594 | C | T | intron_variant | MODIFIER | c.855-63G>A| |
S15 S3 |
16 | BAA03g38960 | A03 | 18076748 | G | A | missense_variant | MODERATE | c.850C>T|p.Arg284Cys |
S271 |
17 | BAA03g38960 | A03 | 18076765 | C | T | missense_variant | MODERATE | c.833G>A|p.Gly278Asp |
S116 |
18 | BAA03g38960 | A03 | 18076998 | C | T | missense_variant | MODERATE | c.740G>A|p.Gly247Asp |
S38 |
19 | BAA03g38960 | A03 | 18077523 | G | A | missense_variant | MODERATE | c.398C>T|p.Ala133Val |
S12 |
20 | BAA03g38960 | A03 | 18078833 | C | T | upstream_gene_variant | MODIFIER | c.-148G>A| |
S155 S211 |
21 | BAA03g38960 | A03 | 18079227 | G | A | upstream_gene_variant | MODIFIER | c.-542C>T| |
S115 |
22 | BAA03g38960 | A03 | 18079230 | C | T | upstream_gene_variant | MODIFIER | c.-545G>A| |
S163 |
23 | BAA03g38960 | A03 | 18079999 | G | A | upstream_gene_variant | MODIFIER | c.-1314C>T| |
S6 |
24 | BAA03g38960 | A03 | 18080100 | C | T | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S34 |
25 | BAA03g38960 | A03 | 18080349 | G | A | upstream_gene_variant | MODIFIER | c.-1664C>T| |
S212 |