| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 26551 | BAA01g18900 | A01 | 9289121 | G | A | downstream_gene_variant | MODIFIER | c.*4288G>A| |
S297 |
| 26552 | BAA01g18910 | A01 | 9291255 | G | T | downstream_gene_variant | MODIFIER | c.*3476G>T| |
S238 |
| 26553 | BAA01g18940 | A01 | 9291712 | C | T | upstream_gene_variant | MODIFIER | c.-4731C>T| |
S150 |
| 26554 | BAA01g18940 | A01 | 9291848 | G | A | upstream_gene_variant | MODIFIER | c.-4595G>A| |
S37 |
| 26555 | BAA01g18920 | A01 | 9292847 | C | T | upstream_gene_variant | MODIFIER | c.-60G>A| |
S170 |
| 26556 | BAA01g18930 | A01 | 9293221 | G | A | synonymous_variant | LOW | c.2689C>T|p.Leu897Leu |
S257 |
| 26557 | BAA01g18930 | A01 | 9293261 | C | T | synonymous_variant | LOW | c.2649G>A|p.Gln883Gln |
S225 |
| 26558 | BAA01g18930 | A01 | 9293435 | C | T | synonymous_variant | LOW | c.2475G>A|p.Val825Val |
S213 |
| 26559 | BAA01g18930 | A01 | 9294164 | G | A | synonymous_variant | LOW | c.1746C>T|p.Tyr582Tyr |
S240 |
| 26560 | BAA01g18930 | A01 | 9294235 | C | T | missense_variant | MODERATE | c.1675G>A|p.Asp559Asn |
S266 |
| 26561 | BAA01g18930 | A01 | 9294502 | C | T | missense_variant | MODERATE | c.1408G>A|p.Ala470Thr |
S25 |
| 26562 | BAA01g18930 | A01 | 9294970 | G | A | missense_variant | MODERATE | c.940C>T|p.Leu314Phe |
S1 S90 |
| 26563 | BAA01g18930 | A01 | 9295089 | C | T | missense_variant | MODERATE | c.821G>A|p.Arg274Lys |
S80 |
| 26564 | BAA01g18930 | A01 | 9295721 | G | A | synonymous_variant | LOW | c.189C>T|p.Val63Val |
S79 S91 |
| 26565 | BAA01g18920 | A01 | 9296009 | G | A | upstream_gene_variant | MODIFIER | c.-3222C>T| |
S57 |
| 26566 | BAA01g18940 | A01 | 9297061 | G | A | missense_variant&splice_region_variant | MODERATE | c.220G>A|p.Glu74Lys |
S281 |
| 26567 | BAA01g18940 | A01 | 9297401 | G | A | synonymous_variant | LOW | c.294G>A|p.Glu98Glu |
S127 |
| 26568 | BAA01g18950 | A01 | 9299008 | C | T | missense_variant | MODERATE | c.1244G>A|p.Ser415Asn |
S247 |
| 26569 | BAA01g18950 | A01 | 9299172 | G | A | missense_variant | MODERATE | c.1171C>T|p.Pro391Ser |
S94 |
| 26570 | BAA01g18970 | A01 | 9301281 | C | T | upstream_gene_variant | MODIFIER | c.-4175C>T| |
S259 |
| 26571 | BAA01g18950 | A01 | 9301590 | G | A | synonymous_variant | LOW | c.111C>T|p.Phe37Phe |
S204 |
| 26572 | BAA01g18950 | A01 | 9301619 | G | A | missense_variant | MODERATE | c.82C>T|p.His28Tyr |
S1 S90 |
| 26573 | BAA01g18950 | A01 | 9302320 | G | A | upstream_gene_variant | MODIFIER | c.-620C>T| |
S173 |
| 26574 | BAA01g18960 | A01 | 9303155 | G | A | missense_variant | MODERATE | c.794C>T|p.Pro265Leu |
S157 S163 |
| 26575 | BAA01g18950 | A01 | 9303432 | G | A | upstream_gene_variant | MODIFIER | c.-1732C>T| |
S40 S49 |