| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 54001 | BAA01g29640 | A01 | 18737024 | C | T | upstream_gene_variant | MODIFIER | c.-3649G>A| |
S7 |
| 54002 | BAA01g29650 | A01 | 18738597 | G | A | intron_variant | MODIFIER | c.1477-157G>A| |
S187 |
| 54003 | BAA01g29650 | A01 | 18738920 | C | T | intron_variant | MODIFIER | c.1619+24C>T| |
S128 |
| 54004 | BAA01g29660 | A01 | 18739663 | G | A | upstream_gene_variant | MODIFIER | c.-4312G>A| |
S199 |
| 54005 | BAA01g29650 | A01 | 18739887 | G | A | missense_variant | MODERATE | c.2044G>A|p.Ala682Thr |
S163 |
| 54006 | BAA01g29650 | A01 | 18741208 | G | A | missense_variant | MODERATE | c.2827G>A|p.Val943Ile |
S259 |
| 54007 | BAA01g29660 | A01 | 18742684 | C | T | upstream_gene_variant | MODIFIER | c.-1291C>T| |
S270 |
| 54008 | BAA01g29660 | A01 | 18742934 | C | T | upstream_gene_variant | MODIFIER | c.-1041C>T| |
S266 |
| 54009 | BAA01g29660 | A01 | 18743070 | C | T | upstream_gene_variant | MODIFIER | c.-905C>T| |
S213 |
| 54010 | BAA01g29660 | A01 | 18744047 | G | A | missense_variant | MODERATE | c.73G>A|p.Ala25Thr |
S246 |
| 54011 | BAA01g29660 | A01 | 18744822 | G | A | missense_variant | MODERATE | c.601G>A|p.Val201Ile |
S116 |
| 54012 | BAA01g29660 | A01 | 18745118 | C | T | missense_variant | MODERATE | c.721C>T|p.Leu241Phe |
S186 |
| 54013 | BAA01g29670 | A01 | 18745723 | G | A | synonymous_variant | LOW | c.1207C>T|p.Leu403Leu |
S202 |
| 54014 | BAA01g29670 | A01 | 18746470 | C | T | missense_variant | MODERATE | c.460G>A|p.Ala154Thr |
S110 |
| 54015 | BAA01g29670 | A01 | 18749831 | C | T | upstream_gene_variant | MODIFIER | c.-2902G>A| |
S112 |
| 54016 | BAA01g29670 | A01 | 18750205 | C | T | upstream_gene_variant | MODIFIER | c.-3276G>A| |
S155 S211 |
| 54017 | BAA01g29670 | A01 | 18750751 | G | A | upstream_gene_variant | MODIFIER | c.-3822C>T| |
S134 |
| 54018 | BAA01g29670 | A01 | 18751137 | C | T | upstream_gene_variant | MODIFIER | c.-4208G>A| |
S64 |
| 54019 | BAA01g29670 | A01 | 18751296 | C | T | upstream_gene_variant | MODIFIER | c.-4367G>A| |
S94 |
| 54020 | BAA01g29680 | A01 | 18751978 | C | T | downstream_gene_variant | MODIFIER | c.*2408G>A| |
S273 |
| 54021 | BAA01g29680 | A01 | 18752774 | C | T | downstream_gene_variant | MODIFIER | c.*1612G>A| |
S210 S225 |
| 54022 | BAA01g29680 | A01 | 18752882 | G | A | downstream_gene_variant | MODIFIER | c.*1504C>T| |
S302 |
| 54023 | BAA01g29680 | A01 | 18753429 | G | A | downstream_gene_variant | MODIFIER | c.*957C>T| |
S151 |
| 54024 | BAA01g29680 | A01 | 18754476 | G | A | synonymous_variant | LOW | c.384C>T|p.Gly128Gly |
S278 |
| 54025 | BAA01g29680 | A01 | 18755124 | C | T | missense_variant | MODERATE | c.217G>A|p.Ala73Thr |
S256 |