Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7701 | BAA01g06170 | A01 | 2768311 | C | T | upstream_gene_variant | MODIFIER | c.-2428G>A| |
S77 S82 |
7702 | BAA01g06170 | A01 | 2769285 | G | A | upstream_gene_variant | MODIFIER | c.-3402C>T| |
S34 |
7703 | BAA01g06180 | A01 | 2769505 | C | T | missense_variant | MODERATE | c.136G>A|p.Glu46Lys |
S282 |
7704 | BAA01g06170 | A01 | 2769771 | G | A | upstream_gene_variant | MODIFIER | c.-3888C>T| |
S134 S193 |
7705 | BAA01g06170 | A01 | 2770313 | C | T | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S211 S227 |
7706 | BAA01g06170 | A01 | 2770549 | G | A | upstream_gene_variant | MODIFIER | c.-4666C>T| |
S191 |
7707 | BAA01g06180 | A01 | 2771780 | C | T | upstream_gene_variant | MODIFIER | c.-2140G>A| |
S299 |
7708 | BAA01g06180 | A01 | 2772963 | G | A | upstream_gene_variant | MODIFIER | c.-3323C>T| |
S157 S163 |
7709 | BAA01g06180 | A01 | 2773140 | C | T | upstream_gene_variant | MODIFIER | c.-3500G>A| |
S206 S26 |
7710 | BAA01g06180 | A01 | 2773298 | G | A | upstream_gene_variant | MODIFIER | c.-3658C>T| |
S15 S3 |
7711 | BAA01g06190 | A01 | 2774983 | G | A | missense_variant | MODERATE | c.350C>T|p.Ser117Phe |
S170 |
7712 | BAA01g06190 | A01 | 2775743 | G | A | upstream_gene_variant | MODIFIER | c.-411C>T| |
S63 |
7713 | BAA01g06190 | A01 | 2776142 | C | T | upstream_gene_variant | MODIFIER | c.-810G>A| |
S68 |
7714 | BAA01g06190 | A01 | 2776423 | G | A | upstream_gene_variant | MODIFIER | c.-1091C>T| |
S133 |
7715 | BAA01g06190 | A01 | 2776598 | G | A | upstream_gene_variant | MODIFIER | c.-1266C>T| |
S150 |
7716 | BAA01g06190 | A01 | 2776698 | C | T | upstream_gene_variant | MODIFIER | c.-1366G>A| |
S247 |
7717 | BAA01g06200 | A01 | 2777202 | G | A | synonymous_variant | LOW | c.93G>A|p.Gln31Gln |
S188 |
7718 | BAA01g06210 | A01 | 2778543 | C | T | missense_variant | MODERATE | c.1765G>A|p.Gly589Ser |
S251 |
7719 | BAA01g06210 | A01 | 2779065 | G | A | synonymous_variant | LOW | c.1243C>T|p.Leu415Leu |
S23 |
7720 | BAA01g06210 | A01 | 2779462 | C | T | splice_region_variant&synonymous_variant | LOW | c.912G>A|p.Lys304Lys |
S166 |
7721 | BAA01g06210 | A01 | 2779887 | C | T | missense_variant | MODERATE | c.487G>A|p.Gly163Arg |
S143 |
7722 | BAA01g06210 | A01 | 2780502 | G | A | missense_variant | MODERATE | c.28C>T|p.Pro10Ser |
S33 |
7723 | BAA01g06210 | A01 | 2780556 | G | A | upstream_gene_variant | MODIFIER | c.-27C>T| |
S15 S3 |
7724 | BAA01g06210 | A01 | 2780950 | C | T | upstream_gene_variant | MODIFIER | c.-421G>A| |
S244 |
7725 | BAA01g06210 | A01 | 2781398 | G | A | upstream_gene_variant | MODIFIER | c.-869C>T| |
S9 |