| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154701 | BAA02g02910 | A02 | 1312660 | G | A | upstream_gene_variant | MODIFIER | c.-3783C>T| |
S59 |
| 154702 | BAA02g02940 | A02 | 1315091 | C | T | missense_variant | MODERATE | c.182C>T|p.Pro61Leu |
S37 |
| 154703 | BAA02g02940 | A02 | 1315187 | G | A | missense_variant | MODERATE | c.278G>A|p.Gly93Glu |
S36 |
| 154704 | BAA02g02950 | A02 | 1316482 | C | T | upstream_gene_variant | MODIFIER | c.-283C>T| |
S2 |
| 154705 | BAA02g02950 | A02 | 1316826 | C | T | missense_variant | MODERATE | c.62C>T|p.Pro21Leu |
S120 |
| 154706 | BAA02g02960 | A02 | 1317596 | C | T | synonymous_variant | LOW | c.792G>A|p.Gln264Gln |
S33 |
| 154707 | BAA02g02960 | A02 | 1317762 | C | T | missense_variant | MODERATE | c.626G>A|p.Gly209Glu |
S283 |
| 154708 | BAA02g02960 | A02 | 1317800 | C | T | synonymous_variant | LOW | c.588G>A|p.Gln196Gln |
S201 |
| 154709 | BAA02g02960 | A02 | 1318489 | G | A | upstream_gene_variant | MODIFIER | c.-28C>T| |
S273 |
| 154710 | BAA02g02960 | A02 | 1319520 | C | T | upstream_gene_variant | MODIFIER | c.-1059G>A| |
S202 |
| 154711 | BAA02g02960 | A02 | 1320130 | G | A | upstream_gene_variant | MODIFIER | c.-1669C>T| |
S173 |
| 154712 | BAA02g02970 | A02 | 1320353 | C | T | missense_variant | MODERATE | c.41G>A|p.Gly14Glu |
S97 |
| 154713 | BAA02g02960 | A02 | 1320483 | G | A | upstream_gene_variant | MODIFIER | c.-2022C>T| |
S191 |
| 154714 | BAA02g02960 | A02 | 1320603 | C | T | upstream_gene_variant | MODIFIER | c.-2142G>A| |
S1 S90 |
| 154715 | BAA02g02960 | A02 | 1321318 | T | A | upstream_gene_variant | MODIFIER | c.-2857A>T| |
S38 |
| 154716 | BAA02g02960 | A02 | 1321504 | C | T | upstream_gene_variant | MODIFIER | c.-3043G>A| |
S175 |
| 154717 | BAA02g02960 | A02 | 1322776 | C | T | upstream_gene_variant | MODIFIER | c.-4315G>A| |
S42 |
| 154718 | BAA02g02970 | A02 | 1324041 | C | T | upstream_gene_variant | MODIFIER | c.-3648G>A| |
S178 |
| 154719 | BAA02g02980 | A02 | 1324175 | G | A | missense_variant | MODERATE | c.1222G>A|p.Glu408Lys |
S266 |
| 154720 | BAA02g02980 | A02 | 1324180 | G | A | synonymous_variant | LOW | c.1227G>A|p.Lys409Lys |
S7 |
| 154721 | BAA02g02980 | A02 | 1324426 | G | A | missense_variant | MODERATE | c.1361G>A|p.Ser454Asn |
S226 |
| 154722 | BAA02g02980 | A02 | 1324431 | G | A | missense_variant | MODERATE | c.1366G>A|p.Val456Met |
S236 |
| 154723 | BAA02g02980 | A02 | 1325678 | G | A | missense_variant | MODERATE | c.2078G>A|p.Arg693Lys |
S134 |
| 154724 | BAA02g02980 | A02 | 1325808 | G | A | missense_variant | MODERATE | c.2141G>A|p.Gly714Asp |
S10 |
| 154725 | BAA02g02980 | A02 | 1326098 | G | A | synonymous_variant | LOW | c.2349G>A|p.Thr783Thr |
S96 |