Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22900 | A07 | 27016502 | C | T | missense_variant | MODERATE | c.1564G>A|p.Asp522Asn |
S265 |
2 | BAA07g22900 | A07 | 27016546 | G | A | missense_variant | MODERATE | c.1520C>T|p.Ala507Val |
S278 |
3 | BAA07g22900 | A07 | 27016611 | G | A | synonymous_variant | LOW | c.1455C>T|p.Leu485Leu |
S252 |
4 | BAA07g22900 | A07 | 27017129 | C | T | missense_variant | MODERATE | c.1225G>A|p.Asp409Asn |
S35 |
5 | BAA07g22900 | A07 | 27017161 | T | C | missense_variant | MODERATE | c.1193A>G|p.Glu398Gly |
S172 |
6 | BAA07g22900 | A07 | 27019586 | C | T | synonymous_variant | LOW | c.270G>A|p.Leu90Leu |
S167 |
7 | BAA07g22900 | A07 | 27020407 | C | T | upstream_gene_variant | MODIFIER | c.-386G>A| |
S192 |
8 | BAA07g22900 | A07 | 27020475 | G | A | upstream_gene_variant | MODIFIER | c.-454C>T| |
S263 |
9 | BAA07g22900 | A07 | 27020589 | C | T | upstream_gene_variant | MODIFIER | c.-568G>A| |
S156 |
10 | BAA07g22900 | A07 | 27020812 | C | T | upstream_gene_variant | MODIFIER | c.-791G>A| |
S148 S210 |
11 | BAA07g22900 | A07 | 27021411 | G | A | upstream_gene_variant | MODIFIER | c.-1390C>T| |
S51 |
12 | BAA07g22900 | A07 | 27021518 | G | A | upstream_gene_variant | MODIFIER | c.-1497C>T| |
S118 |
13 | BAA07g22900 | A07 | 27023546 | C | T | upstream_gene_variant | MODIFIER | c.-3525G>A| |
S61 |
14 | BAA07g22900 | A07 | 27023921 | G | A | upstream_gene_variant | MODIFIER | c.-3900C>T| |
S210 |
15 | BAA07g22900 | A07 | 27024225 | G | A | upstream_gene_variant | MODIFIER | c.-4204C>T| |
S238 |
16 | BAA07g22900 | A07 | 27024813 | G | A | upstream_gene_variant | MODIFIER | c.-4792C>T| |
S308 |