Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4801 | BAA01g03880 | A01 | 1758791 | C | T | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S137 S215 |
4802 | BAA01g03880 | A01 | 1760052 | G | A | upstream_gene_variant | MODIFIER | c.-1691G>A| |
S224 |
4803 | BAA01g03880 | A01 | 1762124 | C | T | stop_gained | HIGH | c.382C>T|p.Gln128* |
S223 |
4804 | BAA01g03880 | A01 | 1762555 | C | T | synonymous_variant | LOW | c.813C>T|p.Val271Val |
S257 |
4805 | BAA01g03890 | A01 | 1763386 | C | T | upstream_gene_variant | MODIFIER | c.-4578C>T| |
S88 |
4806 | BAA01g03880 | A01 | 1764960 | G | A | synonymous_variant | LOW | c.1584G>A|p.Gly528Gly |
S240 |
4807 | BAA01g03880 | A01 | 1765022 | G | A | missense_variant | MODERATE | c.1646G>A|p.Gly549Glu |
S172 S217 |
4808 | BAA01g03880 | A01 | 1765375 | G | A | missense_variant | MODERATE | c.1999G>A|p.Gly667Ser |
S289 S290 |
4809 | BAA01g03890 | A01 | 1765461 | G | A | upstream_gene_variant | MODIFIER | c.-2503G>A| |
S251 |
4810 | BAA01g03890 | A01 | 1765804 | G | A | upstream_gene_variant | MODIFIER | c.-2160G>A| |
S274 |
4811 | BAA01g03890 | A01 | 1766538 | C | T | upstream_gene_variant | MODIFIER | c.-1426C>T| |
S19 |
4812 | BAA01g03890 | A01 | 1767635 | G | A | upstream_gene_variant | MODIFIER | c.-329G>A| |
S7 |
4813 | BAA01g03890 | A01 | 1768016 | G | A | missense_variant | MODERATE | c.53G>A|p.Ser18Asn |
S306 S308 |
4814 | BAA01g03890 | A01 | 1768039 | C | T | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S246 |
4815 | BAA01g03890 | A01 | 1768097 | C | T | missense_variant | MODERATE | c.134C>T|p.Ser45Phe |
S244 |
4816 | BAA01g03890 | A01 | 1768130 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S43 |
4817 | BAA01g03890 | A01 | 1768199 | C | T | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S53 |
4818 | BAA01g03890 | A01 | 1768356 | C | T | synonymous_variant | LOW | c.393C>T|p.Asp131Asp |
S155 S211 |
4819 | BAA01g03890 | A01 | 1771683 | G | A | downstream_gene_variant | MODIFIER | c.*2643G>A| |
S250 |
4820 | BAA01g03910 | A01 | 1772323 | G | A | missense_variant | MODERATE | c.296C>T|p.Pro99Leu |
S184 S190 |
4821 | BAA01g03910 | A01 | 1772593 | C | T | splice_region_variant&intron_variant | LOW | c.175-4G>A| |
S134 |
4822 | BAA01g03910 | A01 | 1773404 | G | A | upstream_gene_variant | MODIFIER | c.-219C>T| |
S169 |
4823 | BAA01g03920 | A01 | 1774563 | G | A | missense_variant | MODERATE | c.610C>T|p.Arg204Trp |
S125 S149 |
4824 | BAA01g03920 | A01 | 1774998 | G | A | missense_variant | MODERATE | c.251C>T|p.Ser84Phe |
S162 |
4825 | BAA01g03910 | A01 | 1775262 | C | T | upstream_gene_variant | MODIFIER | c.-2077G>A| |
S236 |