| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140151 | BAA10g25290 | A10 | 20503910 | G | A | missense_variant | MODERATE | c.620C>T|p.Ala207Val |
S252 |
| 140152 | BAA10g25290 | A10 | 20504516 | C | T | synonymous_variant | LOW | c.180G>A|p.Ala60Ala |
S177 |
| 140153 | BAA10g25290 | A10 | 20504541 | G | A | missense_variant | MODERATE | c.155C>T|p.Ser52Phe |
S74 |
| 140154 | BAA10g25280 | A10 | 20504727 | G | A | upstream_gene_variant | MODIFIER | c.-3226C>T| |
S39 |
| 140155 | BAA10g25280 | A10 | 20504971 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S216 |
| 140156 | BAA10g25280 | A10 | 20505193 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S108 |
| 140157 | BAA10g25300 | A10 | 20505982 | C | T | missense_variant | MODERATE | c.883G>A|p.Val295Met |
S46 |
| 140158 | BAA10g25280 | A10 | 20506349 | C | T | upstream_gene_variant | MODIFIER | c.-4848G>A| |
S8 |
| 140159 | BAA10g25300 | A10 | 20507424 | G | A | synonymous_variant | LOW | c.238C>T|p.Leu80Leu |
S159 S243 |
| 140160 | BAA10g25300 | A10 | 20507579 | G | A | missense_variant | MODERATE | c.166C>T|p.Leu56Phe |
S298 |
| 140161 | BAA10g25320 | A10 | 20509996 | C | T | missense_variant | MODERATE | c.1975G>A|p.Glu659Lys |
S104 S52 |
| 140162 | BAA10g25320 | A10 | 20510316 | C | T | missense_variant | MODERATE | c.1655G>A|p.Arg552Lys |
S224 |
| 140163 | BAA10g25320 | A10 | 20511241 | C | T | missense_variant | MODERATE | c.730G>A|p.Asp244Asn |
S157 |
| 140164 | BAA10g25300 | A10 | 20512417 | C | T | upstream_gene_variant | MODIFIER | c.-4673G>A| |
S218 |
| 140165 | BAA10g25300 | A10 | 20512614 | G | A | upstream_gene_variant | MODIFIER | c.-4870C>T| |
S62 |
| 140166 | BAA10g25330 | A10 | 20512764 | C | T | upstream_gene_variant | MODIFIER | c.-4363C>T| |
S292 |
| 140167 | BAA10g25320 | A10 | 20513344 | C | T | missense_variant | MODERATE | c.86G>A|p.Gly29Glu |
S187 S188 S299 |
| 140168 | BAA10g25320 | A10 | 20513612 | G | A | upstream_gene_variant | MODIFIER | c.-183C>T| |
S250 |
| 140169 | BAA10g25320 | A10 | 20514005 | C | T | upstream_gene_variant | MODIFIER | c.-576G>A| |
S140 |
| 140170 | BAA10g25330 | A10 | 20517475 | C | T | missense_variant | MODERATE | c.104C>T|p.Ser35Leu |
S277 |
| 140171 | BAA10g25330 | A10 | 20517535 | G | A | missense_variant | MODERATE | c.164G>A|p.Ser55Asn |
S289 S290 |
| 140172 | BAA10g25330 | A10 | 20519609 | G | A | splice_region_variant&synonymous_variant | LOW | c.990G>A|p.Glu330Glu |
S126 |
| 140173 | BAA10g25330 | A10 | 20520110 | G | A | missense_variant | MODERATE | c.1189G>A|p.Gly397Arg |
S180 |
| 140174 | BAA10g25330 | A10 | 20520691 | G | A | missense_variant&splice_region_variant | MODERATE | c.1406G>A|p.Gly469Asp |
S90 |
| 140175 | BAA10g25350 | A10 | 20521499 | C | T | upstream_gene_variant | MODIFIER | c.-2396C>T| |
S177 |