| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 9451 | BAA01g07680 | A01 | 3377560 | C | T | downstream_gene_variant | MODIFIER | c.*1541C>T| |
S71 |
| 9452 | BAA01g07700 | A01 | 3378283 | C | T | missense_variant | MODERATE | c.199G>A|p.Asp67Asn |
S114 |
| 9453 | BAA01g07700 | A01 | 3378667 | C | T | upstream_gene_variant | MODIFIER | c.-68G>A| |
S58 |
| 9454 | BAA01g07700 | A01 | 3379045 | G | A | upstream_gene_variant | MODIFIER | c.-446C>T| |
S159 S243 |
| 9455 | BAA01g07700 | A01 | 3379752 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S249 |
| 9456 | BAA01g07700 | A01 | 3381003 | C | T | upstream_gene_variant | MODIFIER | c.-2404G>A| |
S266 |
| 9457 | BAA01g07720 | A01 | 3381392 | C | T | missense_variant | MODERATE | c.2191G>A|p.Gly731Ser |
S39 |
| 9458 | BAA01g07730 | A01 | 3385866 | G | A | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S257 |
| 9459 | BAA01g07730 | A01 | 3385922 | C | T | missense_variant | MODERATE | c.398G>A|p.Gly133Glu |
S125 |
| 9460 | BAA01g07720 | A01 | 3387351 | G | T | upstream_gene_variant | MODIFIER | c.-2559C>A| |
S228 |
| 9461 | BAA01g07720 | A01 | 3387534 | C | T | upstream_gene_variant | MODIFIER | c.-2742G>A| |
S136 |
| 9462 | BAA01g07720 | A01 | 3388719 | G | A | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S174 S27 |
| 9463 | BAA01g07750 | A01 | 3389699 | G | A | missense_variant | MODERATE | c.359G>A|p.Ser120Asn |
S174 S216 S27 S39 |
| 9464 | BAA01g07750 | A01 | 3389853 | G | A | synonymous_variant | LOW | c.513G>A|p.Val171Val |
S115 |
| 9465 | BAA01g07750 | A01 | 3390040 | G | A | missense_variant | MODERATE | c.700G>A|p.Glu234Lys |
S224 |
| 9466 | BAA01g07750 | A01 | 3390132 | C | T | synonymous_variant | LOW | c.792C>T|p.Ile264Ile |
S221 |
| 9467 | BAA01g07750 | A01 | 3390827 | C | T | missense_variant | MODERATE | c.1487C>T|p.Ser496Phe |
S164 |
| 9468 | BAA01g07750 | A01 | 3390890 | C | T | missense_variant | MODERATE | c.1550C>T|p.Ser517Phe |
S218 |
| 9469 | BAA01g07750 | A01 | 3391299 | G | A | synonymous_variant | LOW | c.1959G>A|p.Lys653Lys |
S63 |
| 9470 | BAA01g07760 | A01 | 3393931 | C | T | splice_region_variant&intron_variant | LOW | c.621+7C>T| |
S299 |
| 9471 | BAA01g07760 | A01 | 3394506 | G | A | missense_variant | MODERATE | c.1021G>A|p.Glu341Lys |
S280 |
| 9472 | BAA01g07760 | A01 | 3394809 | G | A | synonymous_variant | LOW | c.1227G>A|p.Lys409Lys |
S190 |
| 9473 | BAA01g07760 | A01 | 3395039 | C | T | missense_variant | MODERATE | c.1457C>T|p.Ser486Phe |
S184 |
| 9474 | BAA01g07760 | A01 | 3395303 | C | A | stop_gained | HIGH | c.1721C>A|p.Ser574* |
S305 |
| 9475 | BAA01g07770 | A01 | 3396981 | G | A | missense_variant | MODERATE | c.511C>T|p.Leu171Phe |
S81 S85 |