Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36500 | A01 | 24437186 | C | T | missense_variant | MODERATE | c.3290G>A|p.Gly1097Glu |
S298 |
2 | BAA01g36500 | A01 | 24437240 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3237-1G>A| |
S242 |
3 | BAA01g36500 | A01 | 24437362 | G | A | synonymous_variant | LOW | c.3201C>T|p.His1067His |
S221 |
4 | BAA01g36500 | A01 | 24437457 | C | T | missense_variant | MODERATE | c.3106G>A|p.Val1036Met |
S164 |
5 | BAA01g36500 | A01 | 24437908 | C | T | intron_variant | MODIFIER | c.2880-131G>A| |
S167 |
6 | BAA01g36500 | A01 | 24438602 | G | A | missense_variant | MODERATE | c.2558C>T|p.Ser853Phe |
S35 |
7 | BAA01g36500 | A01 | 24440379 | C | T | intron_variant | MODIFIER | c.1080-53G>A| |
S305 |
8 | BAA01g36500 | A01 | 24440605 | G | A | missense_variant | MODERATE | c.1028C>T|p.Ser343Phe |
S5 |
9 | BAA01g36500 | A01 | 24441382 | C | T | missense_variant | MODERATE | c.440G>A|p.Ser147Asn |
S166 |
10 | BAA01g36500 | A01 | 24442226 | G | A | upstream_gene_variant | MODIFIER | c.-308C>T| |
S110 S262 |
11 | BAA01g36500 | A01 | 24445360 | C | T | upstream_gene_variant | MODIFIER | c.-3442G>A| |
S249 |
12 | BAA01g36500 | A01 | 24446204 | G | A | upstream_gene_variant | MODIFIER | c.-4286C>T| |
S197 |
13 | BAA01g36500 | A01 | 24446414 | G | A | upstream_gene_variant | MODIFIER | c.-4496C>T| |
S299 |