| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 125151 | BAA10g14470 | A10 | 15163287 | C | T | upstream_gene_variant | MODIFIER | c.-4051C>T| |
S202 |
| 125152 | BAA10g14470 | A10 | 15163627 | T | C | upstream_gene_variant | MODIFIER | c.-3711T>C| |
S107 |
| 125153 | BAA10g14470 | A10 | 15163689 | C | T | upstream_gene_variant | MODIFIER | c.-3649C>T| |
S6 |
| 125154 | BAA10g14470 | A10 | 15164138 | C | T | upstream_gene_variant | MODIFIER | c.-3200C>T| |
S133 |
| 125155 | BAA10g14470 | A10 | 15164563 | C | T | upstream_gene_variant | MODIFIER | c.-2775C>T| |
S173 |
| 125156 | BAA10g14470 | A10 | 15165546 | C | T | upstream_gene_variant | MODIFIER | c.-1792C>T| |
S96 |
| 125157 | BAA10g14460 | A10 | 15167063 | C | T | upstream_gene_variant | MODIFIER | c.-720G>A| |
S146 |
| 125158 | BAA10g14470 | A10 | 15167351 | G | A | missense_variant | MODERATE | c.14G>A|p.Gly5Glu |
S181 |
| 125159 | BAA10g14470 | A10 | 15167622 | G | A | missense_variant | MODERATE | c.170G>A|p.Gly57Glu |
S94 |
| 125160 | BAA10g14470 | A10 | 15168274 | G | A | synonymous_variant | LOW | c.822G>A|p.Glu274Glu |
S64 |
| 125161 | BAA10g14480 | A10 | 15168940 | G | A | missense_variant | MODERATE | c.2884C>T|p.Pro962Ser |
S293 |
| 125162 | BAA10g14480 | A10 | 15169772 | G | A | missense_variant | MODERATE | c.2417C>T|p.Thr806Ile |
S293 |
| 125163 | BAA10g14460 | A10 | 15169903 | G | A | upstream_gene_variant | MODIFIER | c.-3560C>T| |
S113 |
| 125164 | BAA10g14460 | A10 | 15170047 | G | A | upstream_gene_variant | MODIFIER | c.-3704C>T| |
S62 |
| 125165 | BAA10g14480 | A10 | 15170548 | C | T | missense_variant | MODERATE | c.2117G>A|p.Arg706Lys |
S301 S304 |
| 125166 | BAA10g14480 | A10 | 15170610 | C | T | synonymous_variant | LOW | c.2055G>A|p.Arg685Arg |
S246 |
| 125167 | BAA10g14480 | A10 | 15171464 | C | T | missense_variant | MODERATE | c.1630G>A|p.Asp544Asn |
S146 |
| 125168 | BAA10g14480 | A10 | 15171919 | G | A | missense_variant | MODERATE | c.1358C>T|p.Ser453Phe |
S53 |
| 125169 | BAA10g14480 | A10 | 15172306 | G | A | synonymous_variant | LOW | c.1146C>T|p.Phe382Phe |
S278 |
| 125170 | BAA10g14480 | A10 | 15172774 | G | A | missense_variant | MODERATE | c.848C>T|p.Ser283Phe |
S179 |
| 125171 | BAA10g14480 | A10 | 15173233 | G | A | stop_gained | HIGH | c.565C>T|p.Gln189* |
S40 S49 |
| 125172 | BAA10g14480 | A10 | 15173463 | G | A | missense_variant | MODERATE | c.413C>T|p.Pro138Leu |
S279 |
| 125173 | BAA10g14480 | A10 | 15173926 | G | A | missense_variant | MODERATE | c.145C>T|p.Leu49Phe |
S182 |
| 125174 | BAA10g14490 | A10 | 15174493 | C | T | synonymous_variant | LOW | c.1377G>A|p.Arg459Arg |
S56 |
| 125175 | BAA10g14490 | A10 | 15175695 | G | A | missense_variant | MODERATE | c.428C>T|p.Ser143Leu |
S125 |