Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39510 | A01 | 26266726 | G | A | downstream_gene_variant | MODIFIER | c.*800C>T| |
S110 |
2 | BAA01g39510 | A01 | 26268585 | C | T | missense_variant | MODERATE | c.4423G>A|p.Val1475Met |
S305 |
3 | BAA01g39510 | A01 | 26269218 | C | T | missense_variant | MODERATE | c.3790G>A|p.Glu1264Lys |
S69 |
4 | BAA01g39510 | A01 | 26269266 | G | A | missense_variant | MODERATE | c.3742C>T|p.Leu1248Phe |
S110 |
5 | BAA01g39510 | A01 | 26269494 | G | A | missense_variant | MODERATE | c.3514C>T|p.Leu1172Phe |
S143 |
6 | BAA01g39510 | A01 | 26269593 | G | A | missense_variant | MODERATE | c.3415C>T|p.Leu1139Phe |
S15 S3 |
7 | BAA01g39510 | A01 | 26269741 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3268-1G>A| |
S209 |
8 | BAA01g39510 | A01 | 26270793 | G | A | missense_variant | MODERATE | c.2530C>T|p.Pro844Ser |
S87 |
9 | BAA01g39510 | A01 | 26270811 | C | T | missense_variant | MODERATE | c.2512G>A|p.Glu838Lys |
S148 S210 S30 S31 |
10 | BAA01g39510 | A01 | 26271036 | C | T | missense_variant | MODERATE | c.2287G>A|p.Glu763Lys |
S198 |
11 | BAA01g39510 | A01 | 26271147 | C | T | missense_variant | MODERATE | c.2176G>A|p.Asp726Asn |
S78 |
12 | BAA01g39510 | A01 | 26271219 | C | T | missense_variant | MODERATE | c.2104G>A|p.Glu702Lys |
S208 S219 |
13 | BAA01g39510 | A01 | 26273285 | C | T | missense_variant | MODERATE | c.472G>A|p.Val158Ile |
S57 |
14 | BAA01g39510 | A01 | 26274837 | G | A | upstream_gene_variant | MODIFIER | c.-1081C>T| |
S36 |
15 | BAA01g39510 | A01 | 26278673 | C | T | upstream_gene_variant | MODIFIER | c.-4917G>A| |
S16 |