Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2901 | BAA01g02360 | A01 | 1079341 | C | T | missense_variant | MODERATE | c.425C>T|p.Ser142Phe |
S16 |
2902 | BAA01g02360 | A01 | 1079362 | G | A | missense_variant | MODERATE | c.446G>A|p.Gly149Asp |
S289 S290 |
2903 | BAA01g02360 | A01 | 1079473 | G | A | missense_variant | MODERATE | c.557G>A|p.Arg186Lys |
S165 |
2904 | BAA01g02360 | A01 | 1079721 | C | T | synonymous_variant | LOW | c.718C>T|p.Leu240Leu |
S206 S26 |
2905 | BAA01g02380 | A01 | 1080894 | G | A | upstream_gene_variant | MODIFIER | c.-4473G>A| |
S216 |
2906 | BAA01g02380 | A01 | 1081019 | G | A | upstream_gene_variant | MODIFIER | c.-4348G>A| |
S286 |
2907 | BAA01g02380 | A01 | 1081165 | G | A | upstream_gene_variant | MODIFIER | c.-4202G>A| |
S157 S163 |
2908 | BAA01g02380 | A01 | 1081475 | C | T | upstream_gene_variant | MODIFIER | c.-3892C>T| |
S44 |
2909 | BAA01g02370 | A01 | 1082634 | C | T | upstream_gene_variant | MODIFIER | c.-504G>A| |
S282 |
2910 | BAA01g02370 | A01 | 1083317 | G | A | upstream_gene_variant | MODIFIER | c.-1187C>T| |
S12 |
2911 | BAA01g02370 | A01 | 1085348 | C | T | upstream_gene_variant | MODIFIER | c.-3218G>A| |
S238 |
2912 | BAA01g02380 | A01 | 1085589 | G | A | missense_variant | MODERATE | c.149G>A|p.Gly50Glu |
S140 |
2913 | BAA01g02370 | A01 | 1086370 | C | T | upstream_gene_variant | MODIFIER | c.-4240G>A| |
S252 |
2914 | BAA01g02390 | A01 | 1088503 | C | T | synonymous_variant | LOW | c.15C>T|p.Val5Val |
S45 |
2915 | BAA01g02380 | A01 | 1089678 | G | A | downstream_gene_variant | MODIFIER | c.*3330G>A| |
S232 |
2916 | BAA01g02380 | A01 | 1090018 | G | A | downstream_gene_variant | MODIFIER | c.*3670G>A| |
S123 |
2917 | BAA01g02390 | A01 | 1090119 | C | T | missense_variant | MODERATE | c.695C>T|p.Ala232Val |
S192 |
2918 | BAA01g02380 | A01 | 1090870 | C | T | downstream_gene_variant | MODIFIER | c.*4522C>T| |
S206 S26 |
2919 | BAA01g02380 | A01 | 1090889 | G | A | downstream_gene_variant | MODIFIER | c.*4541G>A| |
S221 |
2920 | BAA01g02400 | A01 | 1091437 | G | A | downstream_gene_variant | MODIFIER | c.*1687C>T| |
S161 |
2921 | BAA01g02390 | A01 | 1091787 | G | A | missense_variant | MODERATE | c.1081G>A|p.Val361Met |
S169 |
2922 | BAA01g02390 | A01 | 1093690 | C | T | downstream_gene_variant | MODIFIER | c.*1077C>T| |
S273 |
2923 | BAA01g02390 | A01 | 1094357 | G | A | downstream_gene_variant | MODIFIER | c.*1744G>A| |
S129 |
2924 | BAA01g02390 | A01 | 1094498 | C | T | downstream_gene_variant | MODIFIER | c.*1885C>T| |
S67 |
2925 | BAA01g02400 | A01 | 1095699 | G | A | synonymous_variant | LOW | c.27C>T|p.Ser9Ser |
S203 |