Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
3651 | BAA01g02920 | A01 | 1340337 | C | T | downstream_gene_variant | MODIFIER | c.*3092G>A| |
S113 |
3652 | BAA01g02910 | A01 | 1340584 | G | A | missense_variant | MODERATE | c.1036C>T|p.Pro346Ser |
S6 |
3653 | BAA01g02910 | A01 | 1340623 | G | A | missense_variant | MODERATE | c.997C>T|p.Leu333Phe |
S56 |
3654 | BAA01g02910 | A01 | 1341057 | G | A | synonymous_variant | LOW | c.633C>T|p.Gly211Gly |
S34 |
3655 | BAA01g02910 | A01 | 1341690 | C | T | missense_variant | MODERATE | c.433G>A|p.Val145Ile |
S69 |
3656 | BAA01g02910 | A01 | 1341779 | G | A | missense_variant | MODERATE | c.344C>T|p.Ser115Phe |
S105 S106 |
3657 | BAA01g02910 | A01 | 1341897 | C | T | missense_variant | MODERATE | c.226G>A|p.Glu76Lys |
S265 |
3658 | BAA01g02910 | A01 | 1342031 | C | T | missense_variant | MODERATE | c.92G>A|p.Arg31His |
S262 |
3659 | BAA01g02910 | A01 | 1342826 | G | A | upstream_gene_variant | MODIFIER | c.-704C>T| |
S286 |
3660 | BAA01g02910 | A01 | 1343148 | G | A | upstream_gene_variant | MODIFIER | c.-1026C>T| |
S162 |
3661 | BAA01g02910 | A01 | 1343338 | C | T | upstream_gene_variant | MODIFIER | c.-1216G>A| |
S117 |
3662 | BAA01g02920 | A01 | 1343513 | G | A | synonymous_variant | LOW | c.1506C>T|p.Ser502Ser |
S259 |
3663 | BAA01g02920 | A01 | 1343608 | C | T | missense_variant | MODERATE | c.1411G>A|p.Glu471Lys |
S128 |
3664 | BAA01g02920 | A01 | 1343885 | G | A | synonymous_variant | LOW | c.1284C>T|p.Ile428Ile |
S56 |
3665 | BAA01g02920 | A01 | 1344032 | C | T | missense_variant | MODERATE | c.1216G>A|p.Val406Ile |
S167 |
3666 | BAA01g02920 | A01 | 1345550 | G | A | missense_variant | MODERATE | c.302C>T|p.Ser101Phe |
S256 |
3667 | BAA01g02910 | A01 | 1346403 | G | A | upstream_gene_variant | MODIFIER | c.-4281C>T| |
S204 |
3668 | BAA01g02930 | A01 | 1347970 | C | T | splice_region_variant&intron_variant | LOW | c.269+6C>T| |
S54 |
3669 | BAA01g02940 | A01 | 1350700 | C | T | missense_variant | MODERATE | c.775G>A|p.Val259Met |
S212 |
3670 | BAA01g02930 | A01 | 1350890 | C | T | downstream_gene_variant | MODIFIER | c.*2048C>T| |
S19 |
3671 | BAA01g02940 | A01 | 1351053 | C | T | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S72 |
3672 | BAA01g02940 | A01 | 1351201 | C | T | splice_region_variant&intron_variant | LOW | c.497+4G>A| |
S185 |
3673 | BAA01g02930 | A01 | 1351562 | C | T | downstream_gene_variant | MODIFIER | c.*2720C>T| |
S249 |
3674 | BAA01g02940 | A01 | 1353020 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S117 |
3675 | BAA01g02950 | A01 | 1354490 | C | T | missense_variant | MODERATE | c.322G>A|p.Gly108Ser |
S158 |