| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 79551 | BAA01g41860 | A01 | 27841647 | C | T | missense_variant | MODERATE | c.307G>A|p.Asp103Asn |
S187 S243 S276 |
| 79552 | BAA01g41850 | A01 | 27842076 | C | T | upstream_gene_variant | MODIFIER | c.-4573G>A| |
S156 |
| 79553 | BAA01g41860 | A01 | 27842633 | G | A | missense_variant | MODERATE | c.107C>T|p.Ser36Phe |
S197 |
| 79554 | BAA01g41860 | A01 | 27843862 | G | A | upstream_gene_variant | MODIFIER | c.-1123C>T| |
S139 |
| 79555 | BAA01g41860 | A01 | 27844171 | C | T | upstream_gene_variant | MODIFIER | c.-1432G>A| |
S260 |
| 79556 | BAA01g41860 | A01 | 27844238 | G | A | upstream_gene_variant | MODIFIER | c.-1499C>T| |
S274 |
| 79557 | BAA01g41870 | A01 | 27844682 | T | G | missense_variant | MODERATE | c.95T>G|p.Leu32Arg |
S111 S280 S298 S72 S9 |
| 79558 | BAA01g41870 | A01 | 27844710 | A | C | synonymous_variant | LOW | c.123A>C|p.Ser41Ser |
S111 S177 |
| 79559 | BAA01g41870 | A01 | 27844975 | G | A | missense_variant | MODERATE | c.388G>A|p.Glu130Lys |
S185 |
| 79560 | BAA01g41870 | A01 | 27845187 | G | A | synonymous_variant | LOW | c.600G>A|p.Ser200Ser |
S194 |
| 79561 | BAA01g41860 | A01 | 27845806 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S217 S248 |
| 79562 | BAA01g41860 | A01 | 27845875 | C | T | upstream_gene_variant | MODIFIER | c.-3136G>A| |
S270 |
| 79563 | BAA01g41860 | A01 | 27846041 | C | T | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S69 |
| 79564 | BAA01g41860 | A01 | 27846855 | G | A | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S51 |
| 79565 | BAA01g41860 | A01 | 27846874 | G | A | upstream_gene_variant | MODIFIER | c.-4135C>T| |
S125 |
| 79566 | BAA01g41880 | A01 | 27849057 | G | A | upstream_gene_variant | MODIFIER | c.-4983G>A| |
S212 |
| 79567 | BAA01g41880 | A01 | 27849186 | G | A | upstream_gene_variant | MODIFIER | c.-4854G>A| |
S152 S207 |
| 79568 | BAA01g41880 | A01 | 27849229 | C | T | upstream_gene_variant | MODIFIER | c.-4811C>T| |
S73 |
| 79569 | BAA01g41880 | A01 | 27849669 | C | T | upstream_gene_variant | MODIFIER | c.-4371C>T| |
S303 |
| 79570 | BAA01g41880 | A01 | 27849861 | A | G | upstream_gene_variant | MODIFIER | c.-4179A>G| |
S108 |
| 79571 | BAA01g41880 | A01 | 27849886 | G | A | upstream_gene_variant | MODIFIER | c.-4154G>A| |
S271 |
| 79572 | BAA01g41880 | A01 | 27853323 | C | T | upstream_gene_variant | MODIFIER | c.-717C>T| |
S23 |
| 79573 | BAA01g41880 | A01 | 27853597 | C | T | upstream_gene_variant | MODIFIER | c.-443C>T| |
S171 |
| 79574 | BAA01g41880 | A01 | 27853966 | C | T | upstream_gene_variant | MODIFIER | c.-74C>T| |
S63 |
| 79575 | BAA01g41880 | A01 | 27854182 | G | A | intron_variant | MODIFIER | c.45+98G>A| |
S217 S248 |