| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 121751 | BAA10g12470 | A10 | 13879712 | G | A | downstream_gene_variant | MODIFIER | c.*2090G>A| |
S278 |
| 121752 | BAA10g12470 | A10 | 13880003 | C | T | downstream_gene_variant | MODIFIER | c.*2381C>T| |
S25 |
| 121753 | BAA10g12480 | A10 | 13881613 | C | T | stop_gained | HIGH | c.984G>A|p.Trp328* |
S142 |
| 121754 | BAA10g12480 | A10 | 13881848 | G | A | missense_variant | MODERATE | c.749C>T|p.Ser250Phe |
S165 |
| 121755 | BAA10g12480 | A10 | 13882631 | C | T | intron_variant | MODIFIER | c.595+85G>A| |
S103 |
| 121756 | BAA10g12480 | A10 | 13883345 | C | T | missense_variant | MODERATE | c.73G>A|p.Asp25Asn |
S270 |
| 121757 | BAA10g12480 | A10 | 13883376 | G | A | synonymous_variant | LOW | c.42C>T|p.Ser14Ser |
S82 S92 |
| 121758 | BAA10g12480 | A10 | 13883854 | C | T | upstream_gene_variant | MODIFIER | c.-437G>A| |
S108 |
| 121759 | BAA10g12480 | A10 | 13885636 | C | T | upstream_gene_variant | MODIFIER | c.-2219G>A| |
S166 |
| 121760 | BAA10g12480 | A10 | 13885865 | C | T | upstream_gene_variant | MODIFIER | c.-2448G>A| |
S225 S73 |
| 121761 | BAA10g12480 | A10 | 13886949 | G | A | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S32 |
| 121762 | BAA10g12490 | A10 | 13889825 | G | A | upstream_gene_variant | MODIFIER | c.-1190G>A| |
S157 S163 |
| 121763 | BAA10g12490 | A10 | 13890389 | G | A | upstream_gene_variant | MODIFIER | c.-626G>A| |
S129 |
| 121764 | BAA10g12490 | A10 | 13890421 | G | A | upstream_gene_variant | MODIFIER | c.-594G>A| |
S134 |
| 121765 | BAA10g12490 | A10 | 13890996 | C | T | upstream_gene_variant | MODIFIER | c.-19C>T| |
S95 |
| 121766 | BAA10g12490 | A10 | 13892029 | G | A | downstream_gene_variant | MODIFIER | c.*357G>A| |
S47 |
| 121767 | BAA10g12490 | A10 | 13893423 | G | A | downstream_gene_variant | MODIFIER | c.*1751G>A| |
S59 |
| 121768 | BAA10g12500 | A10 | 13893481 | C | T | missense_variant | MODERATE | c.1516G>A|p.Ala506Thr |
S96 |
| 121769 | BAA10g12500 | A10 | 13894014 | G | A | missense_variant | MODERATE | c.1069C>T|p.Pro357Ser |
S181 |
| 121770 | BAA10g12500 | A10 | 13894047 | G | A | missense_variant | MODERATE | c.1036C>T|p.Pro346Ser |
S105 S106 |
| 121771 | BAA10g12500 | A10 | 13894297 | G | A | synonymous_variant | LOW | c.786C>T|p.Tyr262Tyr |
S68 |
| 121772 | BAA10g12500 | A10 | 13894800 | C | T | missense_variant | MODERATE | c.374G>A|p.Arg125Lys |
S34 |
| 121773 | BAA10g12500 | A10 | 13895120 | C | T | missense_variant | MODERATE | c.133G>A|p.Gly45Arg |
S84 S93 |
| 121774 | BAA10g12500 | A10 | 13897328 | G | A | upstream_gene_variant | MODIFIER | c.-2076C>T| |
S139 |
| 121775 | BAA10g12500 | A10 | 13898037 | G | A | upstream_gene_variant | MODIFIER | c.-2785C>T| |
S128 |