Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g03350 | A04 | 2047760 | C | T | downstream_gene_variant | MODIFIER | c.*4757G>A| |
S9 |
2 | BAA04g03350 | A04 | 2048433 | G | A | downstream_gene_variant | MODIFIER | c.*4084C>T| |
S308 |
3 | BAA04g03350 | A04 | 2048451 | C | T | downstream_gene_variant | MODIFIER | c.*4066G>A| |
S268 |
4 | BAA04g03350 | A04 | 2048611 | G | A | downstream_gene_variant | MODIFIER | c.*3906C>T| |
S157 S167 S263 |
5 | BAA04g03350 | A04 | 2048951 | C | T | downstream_gene_variant | MODIFIER | c.*3566G>A| |
S286 |
6 | BAA04g03350 | A04 | 2049015 | C | T | downstream_gene_variant | MODIFIER | c.*3502G>A| |
S168 |
7 | BAA04g03350 | A04 | 2050583 | C | T | downstream_gene_variant | MODIFIER | c.*1934G>A| |
S223 |
8 | BAA04g03350 | A04 | 2051286 | C | T | downstream_gene_variant | MODIFIER | c.*1231G>A| |
S144 |
9 | BAA04g03350 | A04 | 2052940 | C | T | synonymous_variant | LOW | c.939G>A|p.Ala313Ala |
S295 |
10 | BAA04g03350 | A04 | 2053044 | C | T | missense_variant | MODERATE | c.835G>A|p.Val279Met |
S268 |
11 | BAA04g03350 | A04 | 2054166 | C | T | synonymous_variant | LOW | c.459G>A|p.Ala153Ala |
S174 S27 |
12 | BAA04g03350 | A04 | 2054236 | C | T | missense_variant | MODERATE | c.389G>A|p.Cys130Tyr |
S187 S222 |
13 | BAA04g03350 | A04 | 2054240 | G | A | missense_variant | MODERATE | c.385C>T|p.His129Tyr |
S230 |
14 | BAA04g03350 | A04 | 2054322 | G | A | synonymous_variant | LOW | c.303C>T|p.Phe101Phe |
S36 |
15 | BAA04g03350 | A04 | 2054431 | C | T | missense_variant | MODERATE | c.194G>A|p.Gly65Glu |
S47 |
16 | BAA04g03350 | A04 | 2056041 | C | T | upstream_gene_variant | MODIFIER | c.-1417G>A| |
S15 S3 |
17 | BAA04g03350 | A04 | 2057425 | A | T | upstream_gene_variant | MODIFIER | c.-2801T>A| |
S11 |