| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 19651 | BAA01g14570 | A01 | 6926306 | C | T | upstream_gene_variant | MODIFIER | c.-1532G>A| |
S179 |
| 19652 | BAA01g14570 | A01 | 6926452 | C | T | upstream_gene_variant | MODIFIER | c.-1678G>A| |
S100 |
| 19653 | BAA01g14570 | A01 | 6926941 | C | T | upstream_gene_variant | MODIFIER | c.-2167G>A| |
S82 S92 |
| 19654 | BAA01g14570 | A01 | 6927110 | T | A | upstream_gene_variant | MODIFIER | c.-2336A>T| |
S265 |
| 19655 | BAA01g14580 | A01 | 6927770 | C | T | missense_variant | MODERATE | c.859G>A|p.Asp287Asn |
S151 S263 |
| 19656 | BAA01g14580 | A01 | 6928058 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.709-1G>A| |
S151 S263 |
| 19657 | BAA01g14580 | A01 | 6928360 | C | T | missense_variant | MODERATE | c.616G>A|p.Ala206Thr |
S179 |
| 19658 | BAA01g14580 | A01 | 6930041 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S126 |
| 19659 | BAA01g14590 | A01 | 6930257 | G | A | missense_variant | MODERATE | c.764C>T|p.Thr255Ile |
S171 |
| 19660 | BAA01g14580 | A01 | 6931651 | G | A | upstream_gene_variant | MODIFIER | c.-2258C>T| |
S297 |
| 19661 | BAA01g14580 | A01 | 6931691 | C | T | upstream_gene_variant | MODIFIER | c.-2298G>A| |
S46 |
| 19662 | BAA01g14580 | A01 | 6931892 | C | T | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S208 S93 |
| 19663 | BAA01g14580 | A01 | 6932206 | C | T | upstream_gene_variant | MODIFIER | c.-2813G>A| |
S46 |
| 19664 | BAA01g14580 | A01 | 6932265 | G | A | upstream_gene_variant | MODIFIER | c.-2872C>T| |
S229 |
| 19665 | BAA01g14580 | A01 | 6932697 | G | A | upstream_gene_variant | MODIFIER | c.-3304C>T| |
S15 S156 S2 S213 S3 S4 S6 |
| 19666 | BAA01g14590 | A01 | 6935974 | G | A | upstream_gene_variant | MODIFIER | c.-4595C>T| |
S23 |
| 19667 | BAA01g14600 | A01 | 6936439 | G | A | intron_variant | MODIFIER | c.840+40C>T| |
S183 |
| 19668 | BAA01g14600 | A01 | 6937674 | G | A | synonymous_variant | LOW | c.267C>T|p.Tyr89Tyr |
S263 |
| 19669 | BAA01g14600 | A01 | 6937699 | G | A | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S67 |
| 19670 | BAA01g14600 | A01 | 6939023 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S51 |
| 19671 | BAA01g14600 | A01 | 6940142 | C | T | upstream_gene_variant | MODIFIER | c.-2202G>A| |
S77 |
| 19672 | BAA01g14600 | A01 | 6940348 | C | T | upstream_gene_variant | MODIFIER | c.-2408G>A| |
S260 |
| 19673 | BAA01g14600 | A01 | 6940773 | G | A | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S209 |
| 19674 | BAA01g14600 | A01 | 6941770 | C | T | upstream_gene_variant | MODIFIER | c.-3830G>A| |
S166 |
| 19675 | BAA01g14600 | A01 | 6942041 | C | T | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S291 |