Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g42960 | A07 | 37035877 | C | T | missense_variant | MODERATE | c.1528G>A|p.Asp510Asn |
S118 |
2 | BAA07g42960 | A07 | 37035900 | C | T | missense_variant | MODERATE | c.1505G>A|p.Ser502Asn |
S13 S168 S219 S279 S64 S72 |
3 | BAA07g42960 | A07 | 37038056 | C | T | missense_variant | MODERATE | c.674G>A|p.Arg225Lys |
S210 |
4 | BAA07g42960 | A07 | 37039387 | G | A | synonymous_variant | LOW | c.39C>T|p.His13His |
S162 |
5 | BAA07g42960 | A07 | 37039566 | C | T | upstream_gene_variant | MODIFIER | c.-141G>A| |
S111 |
6 | BAA07g42960 | A07 | 37039650 | G | A | upstream_gene_variant | MODIFIER | c.-225C>T| |
S169 |
7 | BAA07g42960 | A07 | 37040250 | G | A | upstream_gene_variant | MODIFIER | c.-825C>T| |
S269 |
8 | BAA07g42960 | A07 | 37040854 | G | A | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S165 |
9 | BAA07g42960 | A07 | 37043112 | C | T | upstream_gene_variant | MODIFIER | c.-3687G>A| |
S75 |
10 | BAA07g42960 | A07 | 37043153 | C | T | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S212 |
11 | BAA07g42960 | A07 | 37043359 | G | A | upstream_gene_variant | MODIFIER | c.-3934C>T| |
S107 |