| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 101151 | BAA10g07100 | A10 | 3957652 | G | A | upstream_gene_variant | MODIFIER | c.-972G>A| |
S187 |
| 101152 | BAA10g07100 | A10 | 3958816 | G | A | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S209 |
| 101153 | BAA10g07100 | A10 | 3959372 | G | A | missense_variant | MODERATE | c.749G>A|p.Gly250Glu |
S82 S92 |
| 101154 | BAA10g07100 | A10 | 3959383 | C | T | synonymous_variant | LOW | c.760C>T|p.Leu254Leu |
S294 |
| 101155 | BAA10g07120 | A10 | 3959690 | C | T | upstream_gene_variant | MODIFIER | c.-3717C>T| |
S277 |
| 101156 | BAA10g07100 | A10 | 3960139 | G | A | missense_variant | MODERATE | c.1030G>A|p.Ala344Thr |
S33 |
| 101157 | BAA10g07120 | A10 | 3961266 | G | A | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S33 |
| 101158 | BAA10g07110 | A10 | 3962508 | G | A | splice_region_variant&intron_variant | LOW | c.453+7C>T| |
S148 S30 S31 |
| 101159 | BAA10g07110 | A10 | 3963759 | C | T | upstream_gene_variant | MODIFIER | c.-727G>A| |
S166 |
| 101160 | BAA10g07110 | A10 | 3963930 | G | A | upstream_gene_variant | MODIFIER | c.-898C>T| |
S20 |
| 101161 | BAA10g07120 | A10 | 3964101 | C | T | missense_variant | MODERATE | c.431C>T|p.Thr144Ile |
S139 |
| 101162 | BAA10g07110 | A10 | 3965514 | C | T | upstream_gene_variant | MODIFIER | c.-2482G>A| |
S60 |
| 101163 | BAA10g07110 | A10 | 3966035 | C | T | upstream_gene_variant | MODIFIER | c.-3003G>A| |
S135 |
| 101164 | BAA10g07110 | A10 | 3967907 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S221 |
| 101165 | BAA10g07130 | A10 | 3968398 | G | A | upstream_gene_variant | MODIFIER | c.-1051C>T| |
S72 S80 |
| 101166 | BAA10g07140 | A10 | 3968540 | G | A | synonymous_variant | LOW | c.279C>T|p.Val93Val |
S38 |
| 101167 | BAA10g07140 | A10 | 3968768 | G | A | missense_variant | MODERATE | c.125C>T|p.Thr42Ile |
S107 |
| 101168 | BAA10g07130 | A10 | 3969773 | G | A | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S33 |
| 101169 | BAA10g07130 | A10 | 3970444 | T | A | upstream_gene_variant | MODIFIER | c.-3097A>T| |
S244 |
| 101170 | BAA10g07130 | A10 | 3971192 | C | T | upstream_gene_variant | MODIFIER | c.-3845G>A| |
S276 |
| 101171 | BAA10g07150 | A10 | 3971257 | C | T | synonymous_variant | LOW | c.123C>T|p.Leu41Leu |
S68 |
| 101172 | BAA10g07150 | A10 | 3971923 | G | A | missense_variant | MODERATE | c.628G>A|p.Glu210Lys |
S178 |
| 101173 | BAA10g07150 | A10 | 3972406 | G | A | missense_variant | MODERATE | c.838G>A|p.Asp280Asn |
S13 |
| 101174 | BAA10g07150 | A10 | 3972421 | G | A | missense_variant | MODERATE | c.853G>A|p.Glu285Lys |
S276 |
| 101175 | BAA10g07150 | A10 | 3972501 | G | A | synonymous_variant | LOW | c.933G>A|p.Lys311Lys |
S306 |