Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
6901 | BAA01g05660 | A01 | 2516207 | C | T | downstream_gene_variant | MODIFIER | c.*2762G>A| |
S150 |
6902 | BAA01g05660 | A01 | 2516342 | C | T | downstream_gene_variant | MODIFIER | c.*2627G>A| |
S208 S93 |
6903 | BAA01g05650 | A01 | 2516815 | C | T | synonymous_variant | LOW | c.180G>A|p.Thr60Thr |
S302 |
6904 | BAA01g05650 | A01 | 2516922 | C | T | missense_variant | MODERATE | c.73G>A|p.Gly25Arg |
S4 |
6905 | BAA01g05650 | A01 | 2518306 | G | A | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S110 |
6906 | BAA01g05670 | A01 | 2521256 | C | T | missense_variant | MODERATE | c.713G>A|p.Gly238Glu |
S205 |
6907 | BAA01g05670 | A01 | 2521367 | G | A | missense_variant | MODERATE | c.602C>T|p.Ser201Phe |
S236 |
6908 | BAA01g05660 | A01 | 2523080 | C | T | upstream_gene_variant | MODIFIER | c.-2554G>A| |
S46 |
6909 | BAA01g05660 | A01 | 2523135 | C | T | upstream_gene_variant | MODIFIER | c.-2609G>A| |
S4 |
6910 | BAA01g05660 | A01 | 2523209 | C | T | upstream_gene_variant | MODIFIER | c.-2683G>A| |
S203 |
6911 | BAA01g05660 | A01 | 2524963 | G | C | upstream_gene_variant | MODIFIER | c.-4437C>G| |
S67 |
6912 | BAA01g05660 | A01 | 2525080 | C | A | upstream_gene_variant | MODIFIER | c.-4554G>T| |
S303 |
6913 | BAA01g05660 | A01 | 2525278 | G | A | upstream_gene_variant | MODIFIER | c.-4752C>T| |
S148 S210 S30 S31 |
6914 | BAA01g05680 | A01 | 2525735 | C | T | missense_variant | MODERATE | c.955G>A|p.Glu319Lys |
S174 S27 |
6915 | BAA01g05670 | A01 | 2526806 | G | A | upstream_gene_variant | MODIFIER | c.-4671C>T| |
S257 |
6916 | BAA01g05670 | A01 | 2526966 | C | T | upstream_gene_variant | MODIFIER | c.-4831G>A| |
S273 |
6917 | BAA01g05670 | A01 | 2526968 | C | T | upstream_gene_variant | MODIFIER | c.-4833G>A| |
S112 |
6918 | BAA01g05690 | A01 | 2528096 | C | T | synonymous_variant | LOW | c.1188G>A|p.Leu396Leu |
S112 |
6919 | BAA01g05690 | A01 | 2528251 | G | A | missense_variant | MODERATE | c.1033C>T|p.Leu345Phe |
S177 |
6920 | BAA01g05680 | A01 | 2528629 | G | A | upstream_gene_variant | MODIFIER | c.-1940C>T| |
S293 |
6921 | BAA01g05680 | A01 | 2528967 | C | T | upstream_gene_variant | MODIFIER | c.-2278G>A| |
S48 |
6922 | BAA01g05690 | A01 | 2530093 | G | A | missense_variant | MODERATE | c.547C>T|p.Pro183Ser |
S170 |
6923 | BAA01g05690 | A01 | 2530541 | G | A | missense_variant | MODERATE | c.262C>T|p.Arg88Trp |
S174 S216 S39 |
6924 | BAA01g05690 | A01 | 2532492 | C | T | upstream_gene_variant | MODIFIER | c.-1161G>A| |
S62 |
6925 | BAA01g05690 | A01 | 2533561 | C | T | upstream_gene_variant | MODIFIER | c.-2230G>A| |
S74 |