Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
601 | BAA01g00460 | A01 | 205587 | C | T | missense_variant | MODERATE | c.1654C>T|p.Leu552Phe |
S278 |
602 | BAA01g00470 | A01 | 207086 | C | T | upstream_gene_variant | MODIFIER | c.-1981C>T| |
S80 |
603 | BAA01g00470 | A01 | 207337 | G | A | upstream_gene_variant | MODIFIER | c.-1730G>A| |
S169 |
604 | BAA01g00470 | A01 | 207577 | C | T | upstream_gene_variant | MODIFIER | c.-1490C>T| |
S269 |
605 | BAA01g00470 | A01 | 209247 | G | A | missense_variant | MODERATE | c.181G>A|p.Val61Ile |
S295 |
606 | BAA01g00480 | A01 | 209608 | C | T | upstream_gene_variant | MODIFIER | c.-1119C>T| |
S79 |
607 | BAA01g00480 | A01 | 210799 | G | A | missense_variant | MODERATE | c.73G>A|p.Gly25Ser |
S152 |
608 | BAA01g00490 | A01 | 211238 | G | A | upstream_gene_variant | MODIFIER | c.-2762G>A| |
S131 |
609 | BAA01g00490 | A01 | 211666 | C | A | upstream_gene_variant | MODIFIER | c.-2334C>A| |
S289 S290 |
610 | BAA01g00490 | A01 | 211721 | G | A | upstream_gene_variant | MODIFIER | c.-2279G>A| |
S84 S93 |
611 | BAA01g00490 | A01 | 212382 | C | T | upstream_gene_variant | MODIFIER | c.-1618C>T| |
S100 |
612 | BAA01g00490 | A01 | 212914 | G | C | upstream_gene_variant | MODIFIER | c.-1086G>C| |
S14 |
613 | BAA01g00480 | A01 | 215298 | G | A | downstream_gene_variant | MODIFIER | c.*4404G>A| |
S181 |
614 | BAA01g00480 | A01 | 215503 | C | T | downstream_gene_variant | MODIFIER | c.*4609C>T| |
S291 |
615 | BAA01g00500 | A01 | 219016 | C | T | upstream_gene_variant | MODIFIER | c.-1798C>T| |
S158 |
616 | BAA01g00500 | A01 | 219257 | C | T | upstream_gene_variant | MODIFIER | c.-1557C>T| |
S203 |
617 | BAA01g00500 | A01 | 221464 | C | T | synonymous_variant | LOW | c.651C>T|p.Val217Val |
S135 |
618 | BAA01g00500 | A01 | 221705 | G | A | missense_variant | MODERATE | c.892G>A|p.Ala298Thr |
S185 |
619 | BAA01g00500 | A01 | 222201 | C | T | missense_variant | MODERATE | c.1388C>T|p.Ser463Phe |
S284 |
620 | BAA01g00500 | A01 | 222378 | G | A | missense_variant | MODERATE | c.1565G>A|p.Arg522Gln |
S104 S52 |
621 | BAA01g00500 | A01 | 222813 | A | C | missense_variant | MODERATE | c.2000A>C|p.Tyr667Ser |
S11 S110 S133 S168 S175 S194 S195 S197 S277 S284 S303 S45 S54 |
622 | BAA01g00500 | A01 | 222815 | A | C | missense_variant | MODERATE | c.2002A>C|p.Ile668Leu |
S110 S133 S168 S175 S195 S303 S45 S54 |
623 | BAA01g00500 | A01 | 223540 | G | A | synonymous_variant | LOW | c.2727G>A|p.Lys909Lys |
S209 |
624 | BAA01g00500 | A01 | 226183 | C | T | downstream_gene_variant | MODIFIER | c.*1785C>T| |
S192 |
625 | BAA01g00500 | A01 | 226263 | C | T | downstream_gene_variant | MODIFIER | c.*1865C>T| |
S135 |