| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 42101 | BAA01g26120 | A01 | 14513795 | G | A | missense_variant | MODERATE | c.1935G>A|p.Met645Ile |
S274 |
| 42102 | BAA01g26140 | A01 | 14514180 | C | T | upstream_gene_variant | MODIFIER | c.-3206C>T| |
S185 |
| 42103 | BAA01g26140 | A01 | 14514199 | G | A | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S278 |
| 42104 | BAA01g26140 | A01 | 14514202 | G | A | upstream_gene_variant | MODIFIER | c.-3184G>A| |
S117 |
| 42105 | BAA01g26120 | A01 | 14514540 | C | T | missense_variant | MODERATE | c.2270C>T|p.Ala757Val |
S55 |
| 42106 | BAA01g26120 | A01 | 14514739 | G | A | missense_variant | MODERATE | c.2469G>A|p.Met823Ile |
S187 |
| 42107 | BAA01g26120 | A01 | 14514764 | G | A | missense_variant | MODERATE | c.2494G>A|p.Val832Ile |
S298 |
| 42108 | BAA01g26120 | A01 | 14514876 | C | T | missense_variant | MODERATE | c.2606C>T|p.Ala869Val |
S249 |
| 42109 | BAA01g26120 | A01 | 14514885 | G | A | missense_variant | MODERATE | c.2615G>A|p.Arg872His |
S58 |
| 42110 | BAA01g26120 | A01 | 14515083 | G | A | missense_variant | MODERATE | c.2813G>A|p.Gly938Glu |
S240 |
| 42111 | BAA01g26120 | A01 | 14515187 | G | A | missense_variant | MODERATE | c.2831G>A|p.Ser944Asn |
S59 |
| 42112 | BAA01g26140 | A01 | 14515595 | C | T | upstream_gene_variant | MODIFIER | c.-1791C>T| |
S270 |
| 42113 | BAA01g26140 | A01 | 14515659 | G | A | upstream_gene_variant | MODIFIER | c.-1727G>A| |
S201 |
| 42114 | BAA01g26130 | A01 | 14516047 | G | A | missense_variant | MODERATE | c.800C>T|p.Thr267Ile |
S126 |
| 42115 | BAA01g26130 | A01 | 14516315 | G | A | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S63 |
| 42116 | BAA01g26130 | A01 | 14516443 | G | A | missense_variant | MODERATE | c.404C>T|p.Ala135Val |
S37 |
| 42117 | BAA01g26130 | A01 | 14516532 | A | T | missense_variant | MODERATE | c.315T>A|p.Asn105Lys |
S13 |
| 42118 | BAA01g26130 | A01 | 14516631 | G | A | synonymous_variant | LOW | c.216C>T|p.Phe72Phe |
S186 |
| 42119 | BAA01g26130 | A01 | 14516896 | G | A | upstream_gene_variant | MODIFIER | c.-50C>T| |
S191 |
| 42120 | BAA01g26130 | A01 | 14517186 | C | T | upstream_gene_variant | MODIFIER | c.-340G>A| |
S242 |
| 42121 | BAA01g26140 | A01 | 14517663 | C | T | synonymous_variant | LOW | c.198C>T|p.Ile66Ile |
S128 |
| 42122 | BAA01g26150 | A01 | 14518172 | G | A | synonymous_variant | LOW | c.30G>A|p.Glu10Glu |
S274 |
| 42123 | BAA01g26150 | A01 | 14518293 | C | T | stop_gained | HIGH | c.151C>T|p.Arg51* |
S260 |
| 42124 | BAA01g26150 | A01 | 14518345 | C | T | missense_variant | MODERATE | c.203C>T|p.Ser68Phe |
S160 |
| 42125 | BAA01g26130 | A01 | 14518814 | C | T | upstream_gene_variant | MODIFIER | c.-1968G>A| |
S51 |