Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1201 | BAA01g00930 | A01 | 412662 | G | A | upstream_gene_variant | MODIFIER | c.-3732C>T| |
S228 |
1202 | BAA01g00930 | A01 | 412717 | C | T | upstream_gene_variant | MODIFIER | c.-3787G>A| |
S302 |
1203 | BAA01g00930 | A01 | 412793 | G | A | upstream_gene_variant | MODIFIER | c.-3863C>T| |
S10 |
1204 | BAA01g00930 | A01 | 412830 | C | T | upstream_gene_variant | MODIFIER | c.-3900G>A| |
|
1205 | BAA01g00930 | A01 | 412949 | G | A | upstream_gene_variant | MODIFIER | c.-4019C>T| |
S159 S243 S276 S298 |
1206 | BAA01g00940 | A01 | 413346 | G | A | missense_variant | MODERATE | c.28G>A|p.Asp10Asn |
S173 |
1207 | BAA01g00940 | A01 | 413977 | C | T | missense_variant | MODERATE | c.659C>T|p.Ser220Phe |
S302 |
1208 | BAA01g00940 | A01 | 414725 | C | T | missense_variant | MODERATE | c.1223C>T|p.Ala408Val |
S130 |
1209 | BAA01g00940 | A01 | 414775 | G | A | missense_variant | MODERATE | c.1273G>A|p.Val425Ile |
S139 |
1210 | BAA01g00950 | A01 | 417515 | C | T | missense_variant | MODERATE | c.1711C>T|p.Leu571Phe |
S276 |
1211 | BAA01g00950 | A01 | 417686 | G | A | missense_variant | MODERATE | c.1882G>A|p.Glu628Lys |
S293 |
1212 | BAA01g00950 | A01 | 417781 | C | T | synonymous_variant | LOW | c.1977C>T|p.Phe659Phe |
S97 |
1213 | BAA01g00950 | A01 | 418104 | G | A | missense_variant | MODERATE | c.2300G>A|p.Gly767Glu |
S15 S3 |
1214 | BAA01g00960 | A01 | 419240 | G | A | upstream_gene_variant | MODIFIER | c.-107G>A| |
S286 |
1215 | BAA01g00960 | A01 | 419752 | C | T | missense_variant | MODERATE | c.241C>T|p.Arg81Cys |
S77 S82 |
1216 | BAA01g00960 | A01 | 420178 | G | A | splice_region_variant&intron_variant | LOW | c.365+8G>A| |
S138 |
1217 | BAA01g00960 | A01 | 421163 | G | A | missense_variant | MODERATE | c.983G>A|p.Arg328Lys |
S87 |
1218 | BAA01g00980 | A01 | 424416 | C | T | upstream_gene_variant | MODIFIER | c.-985C>T| |
S20 |
1219 | BAA01g00980 | A01 | 425175 | C | T | upstream_gene_variant | MODIFIER | c.-226C>T| |
S273 |
1220 | BAA01g00980 | A01 | 425420 | C | T | missense_variant | MODERATE | c.20C>T|p.Ala7Val |
S40 S49 |
1221 | BAA01g00980 | A01 | 425493 | C | T | synonymous_variant | LOW | c.93C>T|p.Ser31Ser |
S137 |
1222 | BAA01g00980 | A01 | 425646 | T | G | synonymous_variant | LOW | c.246T>G|p.Pro82Pro |
S203 |
1223 | BAA01g00980 | A01 | 425692 | G | A | missense_variant | MODERATE | c.292G>A|p.Glu98Lys |
S116 |
1224 | BAA01g00980 | A01 | 425778 | C | T | synonymous_variant | LOW | c.378C>T|p.Leu126Leu |
S62 |
1225 | BAA01g00990 | A01 | 425947 | G | A | upstream_gene_variant | MODIFIER | c.-3059G>A| |
S142 |