Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
6951 | BAA01g05700 | A01 | 2534014 | C | T | splice_region_variant&intron_variant | LOW | c.341-3C>T| |
S35 |
6952 | BAA01g05690 | A01 | 2535080 | G | A | upstream_gene_variant | MODIFIER | c.-3749C>T| |
S162 |
6953 | BAA01g05710 | A01 | 2535279 | G | A | synonymous_variant | LOW | c.2700C>T|p.Tyr900Tyr |
S228 |
6954 | BAA01g05710 | A01 | 2536160 | C | T | missense_variant | MODERATE | c.2218G>A|p.Gly740Arg |
S42 |
6955 | BAA01g05700 | A01 | 2536436 | G | A | downstream_gene_variant | MODIFIER | c.*1665G>A| |
S116 |
6956 | BAA01g05700 | A01 | 2536573 | C | T | downstream_gene_variant | MODIFIER | c.*1802C>T| |
S130 |
6957 | BAA01g05710 | A01 | 2536802 | C | T | synonymous_variant | LOW | c.1800G>A|p.Arg600Arg |
S135 |
6958 | BAA01g05710 | A01 | 2540442 | C | T | upstream_gene_variant | MODIFIER | c.-962G>A| |
S117 |
6959 | BAA01g05710 | A01 | 2540822 | C | T | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S16 |
6960 | BAA01g05710 | A01 | 2542024 | G | A | upstream_gene_variant | MODIFIER | c.-2544C>T| |
S122 |
6961 | BAA01g05720 | A01 | 2542089 | G | A | stop_gained | HIGH | c.649C>T|p.Gln217* |
S241 S265 S27 |
6962 | BAA01g05720 | A01 | 2542274 | C | T | missense_variant | MODERATE | c.553G>A|p.Glu185Lys |
S205 |
6963 | BAA01g05720 | A01 | 2546447 | C | T | upstream_gene_variant | MODIFIER | c.-3242G>A| |
S79 S84 |
6964 | BAA01g05720 | A01 | 2546884 | G | A | upstream_gene_variant | MODIFIER | c.-3679C>T| |
S144 |
6965 | BAA01g05720 | A01 | 2547519 | G | A | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S283 |
6966 | BAA01g05720 | A01 | 2547552 | G | A | upstream_gene_variant | MODIFIER | c.-4347C>T| |
S116 |
6967 | BAA01g05730 | A01 | 2549784 | G | A | downstream_gene_variant | MODIFIER | c.*1588C>T| |
S293 |
6968 | BAA01g05730 | A01 | 2551949 | G | A | synonymous_variant | LOW | c.1669C>T|p.Leu557Leu |
S165 |
6969 | BAA01g05730 | A01 | 2552636 | G | A | synonymous_variant | LOW | c.1338C>T|p.Phe446Phe |
S13 |
6970 | BAA01g05730 | A01 | 2553653 | C | T | missense_variant | MODERATE | c.800G>A|p.Gly267Glu |
S252 |
6971 | BAA01g05730 | A01 | 2553904 | G | A | synonymous_variant | LOW | c.549C>T|p.Leu183Leu |
S280 |
6972 | BAA01g05730 | A01 | 2554422 | G | A | missense_variant | MODERATE | c.31C>T|p.Pro11Ser |
S115 |
6973 | BAA01g05730 | A01 | 2554429 | C | T | synonymous_variant | LOW | c.24G>A|p.Ser8Ser |
S171 |
6974 | BAA01g05730 | A01 | 2555249 | C | T | upstream_gene_variant | MODIFIER | c.-797G>A| |
S164 |
6975 | BAA01g05730 | A01 | 2555378 | G | A | upstream_gene_variant | MODIFIER | c.-926C>T| |
S295 |