Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35290 | A02 | 30312240 | C | T | upstream_gene_variant | MODIFIER | c.-4996C>T| |
S241 |
2 | BAA02g35290 | A02 | 30312363 | G | A | upstream_gene_variant | MODIFIER | c.-4873G>A| |
S185 |
3 | BAA02g35290 | A02 | 30312498 | C | T | upstream_gene_variant | MODIFIER | c.-4738C>T| |
S296 |
4 | BAA02g35290 | A02 | 30313945 | C | T | upstream_gene_variant | MODIFIER | c.-3291C>T| |
S63 |
5 | BAA02g35290 | A02 | 30314067 | G | T | upstream_gene_variant | MODIFIER | c.-3169G>T| |
S15 S216 S232 S48 S61 |
6 | BAA02g35290 | A02 | 30314859 | C | T | upstream_gene_variant | MODIFIER | c.-2377C>T| |
S249 |
7 | BAA02g35290 | A02 | 30315694 | C | T | upstream_gene_variant | MODIFIER | c.-1542C>T| |
S182 |
8 | BAA02g35290 | A02 | 30316569 | C | T | upstream_gene_variant | MODIFIER | c.-667C>T| |
S42 |
9 | BAA02g35290 | A02 | 30316652 | C | T | upstream_gene_variant | MODIFIER | c.-584C>T| |
S260 |
10 | BAA02g35290 | A02 | 30316707 | T | C | upstream_gene_variant | MODIFIER | c.-529T>C| |
S198 |
11 | BAA02g35290 | A02 | 30317228 | G | A | upstream_gene_variant | MODIFIER | c.-8G>A| |
S35 |
12 | BAA02g35290 | A02 | 30317233 | C | T | upstream_gene_variant | MODIFIER | c.-3C>T| |
S238 |
13 | BAA02g35290 | A02 | 30317418 | C | T | synonymous_variant | LOW | c.183C>T|p.Ala61Ala |
S33 |
14 | BAA02g35290 | A02 | 30317636 | C | T | missense_variant | MODERATE | c.401C>T|p.Ser134Leu |
S244 |
15 | BAA02g35290 | A02 | 30317784 | C | T | synonymous_variant | LOW | c.549C>T|p.Val183Val |
S277 |
16 | BAA02g35290 | A02 | 30317829 | G | A | synonymous_variant | LOW | c.594G>A|p.Lys198Lys |
S256 |
17 | BAA02g35290 | A02 | 30317888 | G | A | missense_variant | MODERATE | c.653G>A|p.Arg218Lys |
S20 |
18 | BAA02g35290 | A02 | 30318097 | G | A | missense_variant | MODERATE | c.862G>A|p.Asp288Asn |
S113 |
19 | BAA02g35290 | A02 | 30318218 | C | T | missense_variant | MODERATE | c.983C>T|p.Ala328Val |
S164 |
20 | BAA02g35290 | A02 | 30318241 | G | A | missense_variant | MODERATE | c.1006G>A|p.Glu336Lys |
S153 S213 |
21 | BAA02g35290 | A02 | 30318544 | G | A | missense_variant | MODERATE | c.1309G>A|p.Asp437Asn |
S80 |
22 | BAA02g35290 | A02 | 30318712 | G | A | missense_variant | MODERATE | c.1477G>A|p.Gly493Ser |
S240 |
23 | BAA02g35290 | A02 | 30320078 | C | T | intron_variant | MODIFIER | c.2518-27C>T| |
S305 |
24 | BAA02g35290 | A02 | 30320151 | G | A | missense_variant | MODERATE | c.2564G>A|p.Arg855Lys |
S59 |
25 | BAA02g35290 | A02 | 30320499 | C | T | missense_variant | MODERATE | c.2912C>T|p.Ser971Phe |
S32 |