| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g23690 | A08 | 17437040 | G | A | downstream_gene_variant | MODIFIER | c.*673C>T| |
S115 |
| 2 | BAA08g23690 | A08 | 17437070 | G | A | downstream_gene_variant | MODIFIER | c.*643C>T| |
S280 |
| 3 | BAA08g23690 | A08 | 17437327 | C | T | downstream_gene_variant | MODIFIER | c.*386G>A| |
S215 |
| 4 | BAA08g23690 | A08 | 17439800 | G | A | missense_variant | MODERATE | c.3701C>T|p.Ser1234Phe |
S241 |
| 5 | BAA08g23690 | A08 | 17440738 | C | T | splice_region_variant&intron_variant | LOW | c.2896-7G>A| |
S114 |
| 6 | BAA08g23690 | A08 | 17440843 | C | T | intron_variant | MODIFIER | c.2896-112G>A| |
S295 |
| 7 | BAA08g23690 | A08 | 17441189 | C | T | missense_variant | MODERATE | c.2746G>A|p.Val916Met |
S23 |
| 8 | BAA08g23690 | A08 | 17441364 | C | T | missense_variant | MODERATE | c.2648G>A|p.Gly883Glu |
S212 |
| 9 | BAA08g23690 | A08 | 17442329 | C | T | missense_variant | MODERATE | c.2002G>A|p.Ala668Thr |
S155 |
| 10 | BAA08g23690 | A08 | 17442595 | G | A | synonymous_variant | LOW | c.1842C>T|p.Ile614Ile |
S158 |
| 11 | BAA08g23690 | A08 | 17442599 | G | A | missense_variant | MODERATE | c.1838C>T|p.Ala613Val |
S172 |
| 12 | BAA08g23690 | A08 | 17442643 | C | T | synonymous_variant | LOW | c.1794G>A|p.Glu598Glu |
S161 |
| 13 | BAA08g23690 | A08 | 17442763 | G | A | intron_variant | MODIFIER | c.1737+30C>T| |
S15 S3 |
| 14 | BAA08g23690 | A08 | 17443295 | C | T | missense_variant | MODERATE | c.1423G>A|p.Asp475Asn |
S294 |
| 15 | BAA08g23690 | A08 | 17443436 | G | A | intron_variant | MODIFIER | c.1368+38C>T| |
S87 |
| 16 | BAA08g23690 | A08 | 17443548 | C | T | missense_variant | MODERATE | c.1294G>A|p.Val432Ile |
S103 |
| 17 | BAA08g23690 | A08 | 17444103 | C | T | intron_variant | MODIFIER | c.1051-41G>A| |
S60 |
| 18 | BAA08g23690 | A08 | 17444356 | G | A | intron_variant | MODIFIER | c.1050+86C>T| |
S65 |
| 19 | BAA08g23690 | A08 | 17444611 | G | A | intron_variant | MODIFIER | c.984+55C>T| |
S151 S263 |
| 20 | BAA08g23690 | A08 | 17445625 | C | T | synonymous_variant | LOW | c.684G>A|p.Glu228Glu |
S28 |
| 21 | BAA08g23690 | A08 | 17445981 | C | T | intron_variant | MODIFIER | c.509+24G>A| |
S230 |
| 22 | BAA08g23690 | A08 | 17446152 | C | T | stop_gained | HIGH | c.362G>A|p.Trp121* |
S212 |
| 23 | BAA08g23690 | A08 | 17446489 | C | T | missense_variant | MODERATE | c.112G>A|p.Val38Met |
S189 |
| 24 | BAA08g23690 | A08 | 17446922 | C | T | upstream_gene_variant | MODIFIER | c.-322G>A| |
S166 |
| 25 | BAA08g23690 | A08 | 17447096 | G | A | upstream_gene_variant | MODIFIER | c.-496C>T| |
S298 |