Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
8851 | BAA01g07140 | A01 | 3165248 | C | T | missense_variant | MODERATE | c.3383G>A|p.Gly1128Glu |
S18 |
8852 | BAA01g07140 | A01 | 3165449 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3265-1G>A| |
S184 |
8853 | BAA01g07140 | A01 | 3166539 | C | T | stop_gained | HIGH | c.2849G>A|p.Trp950* |
S210 |
8854 | BAA01g07120 | A01 | 3166641 | G | A | downstream_gene_variant | MODIFIER | c.*4442G>A| |
S162 |
8855 | BAA01g07140 | A01 | 3166779 | G | A | missense_variant | MODERATE | c.2738C>T|p.Thr913Ile |
S116 |
8856 | BAA01g07140 | A01 | 3167062 | C | T | splice_region_variant&intron_variant | LOW | c.2661+7G>A| |
S113 |
8857 | BAA01g07140 | A01 | 3167804 | C | T | synonymous_variant | LOW | c.2490G>A|p.Glu830Glu |
S305 |
8858 | BAA01g07140 | A01 | 3167836 | C | T | missense_variant | MODERATE | c.2458G>A|p.Asp820Asn |
S256 |
8859 | BAA01g07150 | A01 | 3167949 | G | A | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S207 |
8860 | BAA01g07140 | A01 | 3168555 | G | A | missense_variant | MODERATE | c.2177C>T|p.Ala726Val |
S201 |
8861 | BAA01g07140 | A01 | 3169640 | G | A | synonymous_variant | LOW | c.1354C>T|p.Leu452Leu |
S15 S153 S156 S2 S213 S3 S4 S6 |
8862 | BAA01g07140 | A01 | 3169859 | C | T | missense_variant | MODERATE | c.1250G>A|p.Gly417Asp |
S242 |
8863 | BAA01g07140 | A01 | 3170218 | G | A | missense_variant | MODERATE | c.968C>T|p.Ser323Phe |
S284 |
8864 | BAA01g07140 | A01 | 3171080 | C | T | missense_variant | MODERATE | c.173G>A|p.Arg58Lys |
S267 |
8865 | BAA01g07140 | A01 | 3171099 | C | T | missense_variant | MODERATE | c.154G>A|p.Val52Ile |
S25 |
8866 | BAA01g07150 | A01 | 3172247 | C | T | missense_variant | MODERATE | c.277C>T|p.Pro93Ser |
S302 |
8867 | BAA01g07150 | A01 | 3172918 | C | T | synonymous_variant | LOW | c.948C>T|p.Asp316Asp |
S104 S52 |
8868 | BAA01g07150 | A01 | 3173817 | C | T | missense_variant | MODERATE | c.1601C>T|p.Pro534Leu |
S266 |
8869 | BAA01g07150 | A01 | 3173912 | C | T | missense_variant | MODERATE | c.1696C>T|p.Pro566Ser |
S36 |
8870 | BAA01g07160 | A01 | 3176025 | C | T | missense_variant | MODERATE | c.766G>A|p.Glu256Lys |
S291 |
8871 | BAA01g07140 | A01 | 3176153 | C | T | upstream_gene_variant | MODIFIER | c.-4768G>A| |
S187 |
8872 | BAA01g07160 | A01 | 3176796 | C | T | missense_variant | MODERATE | c.316G>A|p.Glu106Lys |
S58 |
8873 | BAA01g07170 | A01 | 3178590 | C | T | missense_variant | MODERATE | c.410C>T|p.Ala137Val |
S305 |
8874 | BAA01g07170 | A01 | 3178700 | C | T | missense_variant | MODERATE | c.520C>T|p.Leu174Phe |
S211 S227 |
8875 | BAA01g07170 | A01 | 3179442 | G | A | synonymous_variant | LOW | c.1185G>A|p.Thr395Thr |
S221 |