Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20640 | A01 | 10195566 | G | A | missense_variant | MODERATE | c.2243C>T|p.Ser748Leu |
S296 |
2 | BAA01g20640 | A01 | 10195668 | C | T | missense_variant | MODERATE | c.2141G>A|p.Arg714Gln |
S256 |
3 | BAA01g20640 | A01 | 10195697 | C | T | synonymous_variant | LOW | c.2112G>A|p.Arg704Arg |
S18 |
4 | BAA01g20640 | A01 | 10195709 | G | A | synonymous_variant | LOW | c.2100C>T|p.His700His |
S75 S81 |
5 | BAA01g20640 | A01 | 10195840 | G | A | missense_variant | MODERATE | c.1969C>T|p.Pro657Ser |
S59 |
6 | BAA01g20640 | A01 | 10195850 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1960-1G>A| |
S85 |
7 | BAA01g20640 | A01 | 10195897 | C | T | intron_variant | MODIFIER | c.1960-48G>A| |
S161 |
8 | BAA01g20640 | A01 | 10196526 | G | A | intron_variant | MODIFIER | c.1874+19C>T| |
S270 |
9 | BAA01g20640 | A01 | 10196671 | C | T | splice_region_variant&intron_variant | LOW | c.1752-4G>A| |
S242 |
10 | BAA01g20640 | A01 | 10196756 | G | A | splice_region_variant&intron_variant | LOW | c.1751+4C>T| |
S173 |
11 | BAA01g20640 | A01 | 10196892 | G | A | missense_variant | MODERATE | c.1619C>T|p.Pro540Leu |
S245 |
12 | BAA01g20640 | A01 | 10197169 | C | T | synonymous_variant | LOW | c.1422G>A|p.Lys474Lys |
S10 |
13 | BAA01g20640 | A01 | 10197425 | C | T | missense_variant | MODERATE | c.1288G>A|p.Val430Ile |
S54 |
14 | BAA01g20640 | A01 | 10197461 | C | T | missense_variant | MODERATE | c.1252G>A|p.Glu418Lys |
S82 S92 |
15 | BAA01g20640 | A01 | 10200075 | G | A | upstream_gene_variant | MODIFIER | c.-331C>T| |
S291 |
16 | BAA01g20640 | A01 | 10201932 | C | T | upstream_gene_variant | MODIFIER | c.-2188G>A| |
S295 |
17 | BAA01g20640 | A01 | 10202223 | C | T | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S112 |
18 | BAA01g20640 | A01 | 10204472 | G | A | upstream_gene_variant | MODIFIER | c.-4728C>T| |
S8 |