Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
8451 | BAA01g06800 | A01 | 3014609 | G | A | missense_variant | MODERATE | c.1409G>A|p.Cys470Tyr |
S172 S217 |
8452 | BAA01g06800 | A01 | 3015080 | C | T | missense_variant | MODERATE | c.1567C>T|p.Pro523Ser |
S164 |
8453 | BAA01g06790 | A01 | 3016144 | C | T | upstream_gene_variant | MODIFIER | c.-4963G>A| |
S40 S49 |
8454 | BAA01g06810 | A01 | 3017275 | G | A | missense_variant | MODERATE | c.5272C>T|p.Pro1758Ser |
S115 |
8455 | BAA01g06810 | A01 | 3017508 | C | T | missense_variant | MODERATE | c.5137G>A|p.Ala1713Thr |
S135 |
8456 | BAA01g06810 | A01 | 3017692 | C | T | stop_gained | HIGH | c.4953G>A|p.Trp1651* |
S265 |
8457 | BAA01g06810 | A01 | 3018312 | G | A | missense_variant | MODERATE | c.4409C>T|p.Ala1470Val |
S292 |
8458 | BAA01g06810 | A01 | 3018332 | C | T | synonymous_variant | LOW | c.4389G>A|p.Gln1463Gln |
S81 S85 |
8459 | BAA01g06810 | A01 | 3018436 | C | T | missense_variant | MODERATE | c.4285G>A|p.Glu1429Lys |
S16 |
8460 | BAA01g06810 | A01 | 3018917 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3805-1G>A| |
S132 S137 S215 |
8461 | BAA01g06810 | A01 | 3019461 | C | T | missense_variant | MODERATE | c.3359G>A|p.Ser1120Asn |
S99 |
8462 | BAA01g06810 | A01 | 3020045 | G | A | synonymous_variant | LOW | c.2775C>T|p.Asp925Asp |
S197 |
8463 | BAA01g06810 | A01 | 3020827 | C | T | missense_variant | MODERATE | c.1993G>A|p.Glu665Lys |
S51 |
8464 | BAA01g06810 | A01 | 3020919 | G | A | missense_variant | MODERATE | c.1901C>T|p.Ser634Phe |
S221 |
8465 | BAA01g06810 | A01 | 3021388 | C | T | missense_variant | MODERATE | c.1432G>A|p.Glu478Lys |
S18 |
8466 | BAA01g06810 | A01 | 3021559 | C | T | missense_variant | MODERATE | c.1261G>A|p.Ala421Thr |
S139 |
8467 | BAA01g06810 | A01 | 3022009 | G | A | missense_variant | MODERATE | c.811C>T|p.Pro271Ser |
S6 |
8468 | BAA01g06810 | A01 | 3022429 | C | T | missense_variant | MODERATE | c.391G>A|p.Asp131Asn |
S104 S52 |
8469 | BAA01g06810 | A01 | 3025055 | G | T | upstream_gene_variant | MODIFIER | c.-2036C>A| |
S280 |
8470 | BAA01g06810 | A01 | 3025917 | C | T | upstream_gene_variant | MODIFIER | c.-2898G>A| |
S246 |
8471 | BAA01g06830 | A01 | 3026790 | C | T | synonymous_variant | LOW | c.345C>T|p.Phe115Phe |
S67 |
8472 | BAA01g06830 | A01 | 3026793 | C | T | synonymous_variant | LOW | c.348C>T|p.Ser116Ser |
S210 S225 |
8473 | BAA01g06830 | A01 | 3026808 | C | T | synonymous_variant | LOW | c.363C>T|p.Leu121Leu |
S18 |
8474 | BAA01g06810 | A01 | 3027247 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S297 |
8475 | BAA01g06820 | A01 | 3028216 | C | T | upstream_gene_variant | MODIFIER | c.-3542G>A| |
S46 |