Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26640 | A04 | 27118701 | C | T | missense_variant | MODERATE | c.4912G>A|p.Asp1638Asn |
S173 |
2 | BAA04g26640 | A04 | 27118710 | G | A | missense_variant | MODERATE | c.4903C>T|p.Leu1635Phe |
S302 |
3 | BAA04g26640 | A04 | 27118762 | A | C | synonymous_variant | LOW | c.4851T>G|p.Pro1617Pro |
S54 |
4 | BAA04g26640 | A04 | 27122369 | G | A | missense_variant | MODERATE | c.3307C>T|p.Pro1103Ser |
S104 |
5 | BAA04g26640 | A04 | 27122426 | C | T | intron_variant | MODIFIER | c.3280-30G>A| |
S32 |
6 | BAA04g26640 | A04 | 27122889 | G | A | missense_variant | MODERATE | c.3071C>T|p.Ser1024Phe |
S184 |
7 | BAA04g26640 | A04 | 27122989 | C | T | missense_variant&splice_region_variant | MODERATE | c.2971G>A|p.Val991Ile |
S95 |
8 | BAA04g26640 | A04 | 27123093 | C | T | splice_region_variant&intron_variant | LOW | c.2968+8G>A| |
S225 S73 |
9 | BAA04g26640 | A04 | 27123133 | C | T | missense_variant | MODERATE | c.2936G>A|p.Arg979His |
S46 |
10 | BAA04g26640 | A04 | 27124340 | C | T | intron_variant | MODIFIER | c.2401+25G>A| |
S64 |
11 | BAA04g26640 | A04 | 27124627 | C | T | intron_variant | MODIFIER | c.2319+113G>A| |
S244 |
12 | BAA04g26640 | A04 | 27127080 | C | T | synonymous_variant | LOW | c.1458G>A|p.Glu486Glu |
S210 |
13 | BAA04g26640 | A04 | 27127154 | C | T | missense_variant | MODERATE | c.1384G>A|p.Glu462Lys |
S244 |
14 | BAA04g26640 | A04 | 27127927 | C | T | intron_variant | MODIFIER | c.1098+24G>A| |
S143 |
15 | BAA04g26640 | A04 | 27129542 | G | A | intron_variant | MODIFIER | c.577+126C>T| |
S56 |
16 | BAA04g26640 | A04 | 27131436 | G | A | synonymous_variant | LOW | c.24C>T|p.Ser8Ser |
S12 |
17 | BAA04g26640 | A04 | 27133105 | C | T | upstream_gene_variant | MODIFIER | c.-1646G>A| |
S292 |
18 | BAA04g26640 | A04 | 27135368 | C | T | upstream_gene_variant | MODIFIER | c.-3909G>A| |
S250 |
19 | BAA04g26640 | A04 | 27135685 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S215 S288 |