Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1051 | BAA01g00780 | A01 | 357654 | G | A | missense_variant | MODERATE | c.151C>T|p.Leu51Phe |
S294 |
1052 | BAA01g00780 | A01 | 360359 | C | T | upstream_gene_variant | MODIFIER | c.-2555G>A| |
S137 |
1053 | BAA01g00780 | A01 | 361256 | G | A | upstream_gene_variant | MODIFIER | c.-3452C>T| |
S168 |
1054 | BAA01g00780 | A01 | 361513 | C | T | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S130 |
1055 | BAA01g00790 | A01 | 363363 | G | A | downstream_gene_variant | MODIFIER | c.*533C>T| |
S7 |
1056 | BAA01g00790 | A01 | 363633 | G | A | downstream_gene_variant | MODIFIER | c.*263C>T| |
S10 |
1057 | BAA01g00790 | A01 | 363864 | G | A | downstream_gene_variant | MODIFIER | c.*32C>T| |
S153 |
1058 | BAA01g00800 | A01 | 364799 | C | T | upstream_gene_variant | MODIFIER | c.-4752C>T| |
S238 |
1059 | BAA01g00790 | A01 | 365669 | G | A | synonymous_variant | LOW | c.693C>T|p.Phe231Phe |
S65 |
1060 | BAA01g00790 | A01 | 365718 | C | T | missense_variant | MODERATE | c.644G>A|p.Arg215Lys |
S52 |
1061 | BAA01g00790 | A01 | 365878 | C | T | missense_variant | MODERATE | c.484G>A|p.Asp162Asn |
S184 |
1062 | BAA01g00790 | A01 | 366683 | G | A | upstream_gene_variant | MODIFIER | c.-322C>T| |
S173 |
1063 | BAA01g00790 | A01 | 366937 | C | T | upstream_gene_variant | MODIFIER | c.-576G>A| |
S302 |
1064 | BAA01g00800 | A01 | 369748 | G | A | synonymous_variant | LOW | c.198G>A|p.Gly66Gly |
S32 |
1065 | BAA01g00790 | A01 | 370648 | G | A | upstream_gene_variant | MODIFIER | c.-4287C>T| |
S129 |
1066 | BAA01g00790 | A01 | 371033 | C | T | upstream_gene_variant | MODIFIER | c.-4672G>A| |
S20 |
1067 | BAA01g00790 | A01 | 371068 | G | A | upstream_gene_variant | MODIFIER | c.-4707C>T| |
S6 |
1068 | BAA01g00810 | A01 | 372042 | C | T | missense_variant | MODERATE | c.1423G>A|p.Gly475Arg |
S107 |
1069 | BAA01g00810 | A01 | 372044 | G | A | missense_variant | MODERATE | c.1421C>T|p.Pro474Leu |
S83 S88 |
1070 | BAA01g00820 | A01 | 372970 | G | A | upstream_gene_variant | MODIFIER | c.-3464G>A| |
S188 |
1071 | BAA01g00810 | A01 | 374536 | G | A | upstream_gene_variant | MODIFIER | c.-85C>T| |
S199 |
1072 | BAA01g00810 | A01 | 375903 | G | A | upstream_gene_variant | MODIFIER | c.-1452C>T| |
S186 |
1073 | BAA01g00830 | A01 | 378948 | G | A | splice_region_variant&stop_retained_variant | LOW | c.320G>A|p.Ter107Ter |
S89 |
1074 | BAA01g00810 | A01 | 379012 | C | T | upstream_gene_variant | MODIFIER | c.-4561G>A| |
S261 |
1075 | BAA01g00820 | A01 | 380056 | C | T | downstream_gene_variant | MODIFIER | c.*3069C>T| |
S193 |