| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 39151 | BAA01g25160 | A01 | 13503778 | G | A | missense_variant | MODERATE | c.320C>T|p.Ser107Phe |
S23 |
| 39152 | BAA01g25160 | A01 | 13504091 | C | T | intron_variant | MODIFIER | c.129+41G>A| |
S4 |
| 39153 | BAA01g25160 | A01 | 13504183 | G | A | synonymous_variant | LOW | c.78C>T|p.Leu26Leu |
S80 |
| 39154 | BAA01g25160 | A01 | 13505151 | C | T | upstream_gene_variant | MODIFIER | c.-891G>A| |
S200 |
| 39155 | BAA01g25160 | A01 | 13506688 | A | G | upstream_gene_variant | MODIFIER | c.-2428T>C| |
S210 |
| 39156 | BAA01g25160 | A01 | 13508199 | G | A | upstream_gene_variant | MODIFIER | c.-3939C>T| |
S142 S251 |
| 39157 | BAA01g25160 | A01 | 13508218 | G | A | upstream_gene_variant | MODIFIER | c.-3958C>T| |
S301 S304 |
| 39158 | BAA01g25160-BAA01g25170 | A01 | 13510788 | C | T | intergenic_region | MODIFIER | n.13510788C>T| |
S213 |
| 39159 | BAA01g25170 | A01 | 13513328 | C | T | downstream_gene_variant | MODIFIER | c.*4339G>A| |
S265 |
| 39160 | BAA01g25170 | A01 | 13515040 | G | A | downstream_gene_variant | MODIFIER | c.*2627C>T| |
S72 |
| 39161 | BAA01g25170 | A01 | 13516377 | G | A | downstream_gene_variant | MODIFIER | c.*1290C>T| |
S78 |
| 39162 | BAA01g25170 | A01 | 13516555 | C | T | downstream_gene_variant | MODIFIER | c.*1112G>A| |
S8 |
| 39163 | BAA01g25170 | A01 | 13516632 | C | T | downstream_gene_variant | MODIFIER | c.*1035G>A| |
S221 |
| 39164 | BAA01g25170 | A01 | 13516989 | G | A | downstream_gene_variant | MODIFIER | c.*678C>T| |
S229 |
| 39165 | BAA01g25170 | A01 | 13517555 | C | T | downstream_gene_variant | MODIFIER | c.*112G>A| |
S128 |
| 39166 | BAA01g25170 | A01 | 13517752 | G | A | missense_variant | MODERATE | c.914C>T|p.Ser305Phe |
S58 |
| 39167 | BAA01g25170 | A01 | 13517827 | G | A | splice_region_variant&intron_variant | LOW | c.847-8C>T| |
S234 |
| 39168 | BAA01g25170 | A01 | 13518703 | G | A | missense_variant | MODERATE | c.470C>T|p.Ser157Phe |
S251 |
| 39169 | BAA01g25170 | A01 | 13520059 | C | T | missense_variant&splice_region_variant | MODERATE | c.275G>A|p.Gly92Glu |
S47 |
| 39170 | BAA01g25170 | A01 | 13520109 | C | T | intron_variant | MODIFIER | c.273-48G>A| |
S242 |
| 39171 | BAA01g25170 | A01 | 13520221 | G | A | intron_variant | MODIFIER | c.273-160C>T| |
S123 |
| 39172 | BAA01g25170 | A01 | 13520293 | C | T | intron_variant | MODIFIER | c.273-232G>A| |
S148 S210 S30 S31 |
| 39173 | BAA01g25170 | A01 | 13520932 | C | T | missense_variant | MODERATE | c.201G>A|p.Met67Ile |
S48 |
| 39174 | BAA01g25170 | A01 | 13521492 | G | A | upstream_gene_variant | MODIFIER | c.-169C>T| |
S62 |
| 39175 | BAA01g25170 | A01 | 13522059 | A | T | upstream_gene_variant | MODIFIER | c.-736T>A| |
S177 |