Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1551 | BAA01g01290 | A01 | 535160 | C | T | upstream_gene_variant | MODIFIER | c.-4324C>T| |
S255 |
1552 | BAA01g01290 | A01 | 538230 | C | T | upstream_gene_variant | MODIFIER | c.-1254C>T| |
S167 S263 |
1553 | BAA01g01290 | A01 | 538696 | C | T | upstream_gene_variant | MODIFIER | c.-788C>T| |
S192 |
1554 | BAA01g01290 | A01 | 541050 | C | T | downstream_gene_variant | MODIFIER | c.*257C>T| |
S54 |
1555 | BAA01g01290 | A01 | 541187 | G | A | downstream_gene_variant | MODIFIER | c.*394G>A| |
S34 |
1556 | BAA01g01290 | A01 | 541274 | G | A | downstream_gene_variant | MODIFIER | c.*481G>A| |
S217 S248 |
1557 | BAA01g01290 | A01 | 541892 | G | A | downstream_gene_variant | MODIFIER | c.*1099G>A| |
S162 |
1558 | BAA01g01290 | A01 | 542529 | G | A | downstream_gene_variant | MODIFIER | c.*1736G>A| |
S108 |
1559 | BAA01g01290 | A01 | 542559 | T | G | downstream_gene_variant | MODIFIER | c.*1766T>G| |
S108 |
1560 | BAA01g01290 | A01 | 542647 | C | T | downstream_gene_variant | MODIFIER | c.*1854C>T| |
S168 |
1561 | BAA01g01290 | A01 | 542978 | C | T | downstream_gene_variant | MODIFIER | c.*2185C>T| |
S90 |
1562 | BAA01g01290 | A01 | 543114 | G | A | downstream_gene_variant | MODIFIER | c.*2321G>A| |
S110 |
1563 | BAA01g01290 | A01 | 543315 | C | T | downstream_gene_variant | MODIFIER | c.*2522C>T| |
S249 |
1564 | BAA01g01290 | A01 | 544166 | C | T | downstream_gene_variant | MODIFIER | c.*3373C>T| |
S218 |
1565 | BAA01g01290-BAA01g01300 | A01 | 546981 | C | T | intergenic_region | MODIFIER | n.546981C>T| |
S8 |
1566 | BAA01g01300 | A01 | 548897 | C | T | upstream_gene_variant | MODIFIER | c.-3106C>T| |
S50 |
1567 | BAA01g01300 | A01 | 549381 | C | T | upstream_gene_variant | MODIFIER | c.-2622C>T| |
S42 |
1568 | BAA01g01300 | A01 | 550247 | G | T | upstream_gene_variant | MODIFIER | c.-1756G>T| |
S183 S198 |
1569 | BAA01g01300 | A01 | 552461 | C | T | synonymous_variant | LOW | c.399C>T|p.Ile133Ile |
S246 |
1570 | BAA01g01310 | A01 | 552839 | C | T | upstream_gene_variant | MODIFIER | c.-2102C>T| |
S305 |
1571 | BAA01g01300 | A01 | 553317 | G | A | missense_variant | MODERATE | c.965G>A|p.Gly322Glu |
S103 |
1572 | BAA01g01300 | A01 | 553596 | G | A | missense_variant&splice_region_variant | MODERATE | c.1154G>A|p.Gly385Glu |
S260 |
1573 | BAA01g01300 | A01 | 553869 | G | A | missense_variant | MODERATE | c.1189G>A|p.Val397Met |
S103 |
1574 | BAA01g01300 | A01 | 553883 | C | T | synonymous_variant | LOW | c.1203C>T|p.Cys401Cys |
S281 |
1575 | BAA01g01300 | A01 | 555448 | G | A | downstream_gene_variant | MODIFIER | c.*1295G>A| |
S294 |