Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
3501 | BAA01g02760 | A01 | 1279322 | C | T | synonymous_variant | LOW | c.432C>T|p.Tyr144Tyr |
S16 S181 S217 S56 |
3502 | BAA01g02750 | A01 | 1280098 | G | A | upstream_gene_variant | MODIFIER | c.-2351C>T| |
S204 |
3503 | BAA01g02750 | A01 | 1280204 | C | T | upstream_gene_variant | MODIFIER | c.-2457G>A| |
S97 |
3504 | BAA01g02750 | A01 | 1280335 | C | T | upstream_gene_variant | MODIFIER | c.-2588G>A| |
S20 |
3505 | BAA01g02770 | A01 | 1281154 | C | T | splice_region_variant&intron_variant | LOW | c.369-5C>T| |
S219 |
3506 | BAA01g02770 | A01 | 1281529 | C | T | synonymous_variant | LOW | c.642C>T|p.Arg214Arg |
S168 |
3507 | BAA01g02750 | A01 | 1281896 | C | T | upstream_gene_variant | MODIFIER | c.-4149G>A| |
S126 |
3508 | BAA01g02750 | A01 | 1282556 | G | A | upstream_gene_variant | MODIFIER | c.-4809C>T| |
S191 |
3509 | BAA01g02780 | A01 | 1282936 | G | A | upstream_gene_variant | MODIFIER | c.-766G>A| |
S296 |
3510 | BAA01g02780 | A01 | 1283145 | C | T | upstream_gene_variant | MODIFIER | c.-557C>T| |
S221 |
3511 | BAA01g02780 | A01 | 1283710 | G | A | synonymous_variant | LOW | c.9G>A|p.Pro3Pro |
S204 |
3512 | BAA01g02770 | A01 | 1286171 | C | T | downstream_gene_variant | MODIFIER | c.*4492C>T| |
S164 |
3513 | BAA01g02780 | A01 | 1286899 | G | A | missense_variant&splice_region_variant | MODERATE | c.1588G>A|p.Val530Met |
S297 |
3514 | BAA01g02780 | A01 | 1287490 | G | A | missense_variant | MODERATE | c.2179G>A|p.Glu727Lys |
S83 S88 |
3515 | BAA01g02780 | A01 | 1287749 | C | T | missense_variant | MODERATE | c.2438C>T|p.Pro813Leu |
S44 |
3516 | BAA01g02780 | A01 | 1287952 | C | T | missense_variant | MODERATE | c.2641C>T|p.Pro881Ser |
S113 |
3517 | BAA01g02780 | A01 | 1288396 | C | T | intron_variant | MODIFIER | c.2821-76C>T| |
S30 S31 |
3518 | BAA01g02780 | A01 | 1290198 | G | A | missense_variant | MODERATE | c.4345G>A|p.Glu1449Lys |
S259 |
3519 | BAA01g02780 | A01 | 1291037 | C | T | splice_region_variant&intron_variant | LOW | c.5004+5C>T| |
S66 |
3520 | BAA01g02780 | A01 | 1292666 | G | A | missense_variant | MODERATE | c.5875G>A|p.Gly1959Ser |
S159 S243 |
3521 | BAA01g02780 | A01 | 1292698 | G | A | synonymous_variant | LOW | c.5907G>A|p.Arg1969Arg |
S95 |
3522 | BAA01g02780 | A01 | 1293255 | C | T | intron_variant | MODIFIER | c.6250-159C>T| |
S240 |
3523 | BAA01g02780 | A01 | 1294053 | C | T | synonymous_variant | LOW | c.6805C>T|p.Leu2269Leu |
S221 |
3524 | BAA01g02780 | A01 | 1294067 | G | A | synonymous_variant | LOW | c.6819G>A|p.Leu2273Leu |
S7 |
3525 | BAA01g02780 | A01 | 1294696 | C | T | missense_variant | MODERATE | c.7190C>T|p.Ser2397Leu |
S182 |