Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41190 | A01 | 27392592 | C | T | upstream_gene_variant | MODIFIER | c.-2078C>T| |
S260 |
2 | BAA01g41190 | A01 | 27393781 | C | T | upstream_gene_variant | MODIFIER | c.-889C>T| |
S132 S215 |
3 | BAA01g41190 | A01 | 27393939 | C | T | upstream_gene_variant | MODIFIER | c.-731C>T| |
S204 |
4 | BAA01g41190 | A01 | 27394041 | C | T | upstream_gene_variant | MODIFIER | c.-629C>T| |
S203 |
5 | BAA01g41190 | A01 | 27394181 | C | T | upstream_gene_variant | MODIFIER | c.-489C>T| |
S166 |
6 | BAA01g41190 | A01 | 27394336 | C | T | upstream_gene_variant | MODIFIER | c.-334C>T| |
S111 |
7 | BAA01g41190 | A01 | 27395985 | C | T | missense_variant | MODERATE | c.725C>T|p.Ser242Phe |
S148 S210 S30 S31 |
8 | BAA01g41190 | A01 | 27396253 | G | A | splice_donor_variant&intron_variant | HIGH | c.916+1G>A| |
S223 |
9 | BAA01g41190 | A01 | 27397350 | C | T | missense_variant | MODERATE | c.1937C>T|p.Ser646Phe |
S132 S215 S89 |
10 | BAA01g41190 | A01 | 27397580 | C | T | missense_variant | MODERATE | c.2087C>T|p.Ser696Phe |
S80 |
11 | BAA01g41190 | A01 | 27398246 | C | T | synonymous_variant | LOW | c.2454C>T|p.Phe818Phe |
S202 |
12 | BAA01g41190 | A01 | 27398919 | C | T | synonymous_variant | LOW | c.2841C>T|p.Ile947Ile |
S128 |
13 | BAA01g41190 | A01 | 27402420 | C | T | downstream_gene_variant | MODIFIER | c.*3197C>T| |
S303 |