Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
3001 | BAA01g02440 | A01 | 1117779 | G | A | upstream_gene_variant | MODIFIER | c.-1108G>A| |
S242 |
3002 | BAA01g02440 | A01 | 1117844 | G | A | upstream_gene_variant | MODIFIER | c.-1043G>A| |
S256 |
3003 | BAA01g02440 | A01 | 1118901 | C | T | synonymous_variant | LOW | c.15C>T|p.Leu5Leu |
S128 |
3004 | BAA01g02440 | A01 | 1119823 | C | T | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S53 |
3005 | BAA01g02440 | A01 | 1120279 | G | A | missense_variant | MODERATE | c.1261G>A|p.Ala421Thr |
S183 S198 |
3006 | BAA01g02440 | A01 | 1120288 | G | A | missense_variant | MODERATE | c.1270G>A|p.Asp424Asn |
S183 S198 |
3007 | BAA01g02440 | A01 | 1120545 | G | A | synonymous_variant | LOW | c.1527G>A|p.Arg509Arg |
S272 |
3008 | BAA01g02440 | A01 | 1121006 | G | A | missense_variant | MODERATE | c.1988G>A|p.Arg663Lys |
S245 |
3009 | BAA01g02440 | A01 | 1121322 | G | A | synonymous_variant | LOW | c.2304G>A|p.Glu768Glu |
S23 |
3010 | BAA01g02440 | A01 | 1121329 | G | A | missense_variant | MODERATE | c.2311G>A|p.Glu771Lys |
S28 |
3011 | BAA01g02440 | A01 | 1122171 | G | A | synonymous_variant | LOW | c.3153G>A|p.Val1051Val |
S80 |
3012 | BAA01g02440 | A01 | 1122174 | G | A | synonymous_variant | LOW | c.3156G>A|p.Glu1052Glu |
S115 |
3013 | BAA01g02450 | A01 | 1123071 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S228 |
3014 | BAA01g02450 | A01 | 1123733 | C | T | synonymous_variant | LOW | c.243C>T|p.Ser81Ser |
S203 |
3015 | BAA01g02460 | A01 | 1124897 | C | T | upstream_gene_variant | MODIFIER | c.-266C>T| |
S192 |
3016 | BAA01g02440 | A01 | 1125637 | G | A | downstream_gene_variant | MODIFIER | c.*2512G>A| |
S14 |
3017 | BAA01g02480 | A01 | 1125731 | G | A | upstream_gene_variant | MODIFIER | c.-4928G>A| |
S33 |
3018 | BAA01g02480 | A01 | 1125837 | C | T | upstream_gene_variant | MODIFIER | c.-4822C>T| |
S107 |
3019 | BAA01g02470 | A01 | 1126652 | C | T | missense_variant | MODERATE | c.709G>A|p.Asp237Asn |
S244 |
3020 | BAA01g02470 | A01 | 1126984 | G | A | synonymous_variant | LOW | c.465C>T|p.Ile155Ile |
S181 |
3021 | BAA01g02470 | A01 | 1127018 | C | T | missense_variant | MODERATE | c.431G>A|p.Gly144Glu |
S252 |
3022 | BAA01g02470 | A01 | 1127787 | C | T | upstream_gene_variant | MODIFIER | c.-257G>A| |
S182 |
3023 | BAA01g02470 | A01 | 1128150 | C | T | upstream_gene_variant | MODIFIER | c.-620G>A| |
S94 |
3024 | BAA01g02470 | A01 | 1130153 | C | T | upstream_gene_variant | MODIFIER | c.-2623G>A| |
S136 |
3025 | BAA01g02470 | A01 | 1130185 | C | A | upstream_gene_variant | MODIFIER | c.-2655G>T| |
S153 S159 S193 S201 S235 S239 |