Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41520 | A02 | 34826226 | C | T | upstream_gene_variant | MODIFIER | c.-3731C>T| |
S277 |
2 | BAA02g41520 | A02 | 34826768 | G | A | upstream_gene_variant | MODIFIER | c.-3189G>A| |
S18 S221 |
3 | BAA02g41520 | A02 | 34828092 | G | A | upstream_gene_variant | MODIFIER | c.-1865G>A| |
S126 |
4 | BAA02g41520 | A02 | 34828321 | C | T | upstream_gene_variant | MODIFIER | c.-1636C>T| |
S17 |
5 | BAA02g41520 | A02 | 34828447 | C | T | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S272 |
6 | BAA02g41520 | A02 | 34829702 | C | T | upstream_gene_variant | MODIFIER | c.-255C>T| |
S295 |
7 | BAA02g41520 | A02 | 34829932 | C | T | upstream_gene_variant | MODIFIER | c.-25C>T| |
S283 |
8 | BAA02g41520 | A02 | 34830176 | G | A | missense_variant | MODERATE | c.220G>A|p.Asp74Asn |
S175 |
9 | BAA02g41520 | A02 | 34830250 | C | T | synonymous_variant | LOW | c.294C>T|p.Leu98Leu |
S183 S198 |
10 | BAA02g41520 | A02 | 34830455 | G | A | missense_variant | MODERATE | c.355G>A|p.Gly119Arg |
S134 |
11 | BAA02g41520 | A02 | 34830497 | G | A | missense_variant | MODERATE | c.397G>A|p.Glu133Lys |
S188 |
12 | BAA02g41520 | A02 | 34830540 | C | T | missense_variant | MODERATE | c.440C>T|p.Ser147Leu |
S202 |
13 | BAA02g41520 | A02 | 34830679 | G | A | stop_gained | HIGH | c.579G>A|p.Trp193* |
S231 |
14 | BAA02g41520 | A02 | 34830734 | C | T | stop_gained | HIGH | c.634C>T|p.Gln212* |
S266 |
15 | BAA02g41520 | A02 | 34831213 | C | T | synonymous_variant | LOW | c.1113C>T|p.Phe371Phe |
S283 |
16 | BAA02g41520 | A02 | 34831344 | G | A | missense_variant | MODERATE | c.1244G>A|p.Arg415Lys |
S194 |
17 | BAA02g41520 | A02 | 34832664 | G | A | missense_variant | MODERATE | c.2081G>A|p.Arg694Lys |
S245 |
18 | BAA02g41520 | A02 | 34837830 | C | T | downstream_gene_variant | MODIFIER | c.*4551C>T| |
S152 |
19 | BAA02g41520 | A02 | 34838178 | G | A | downstream_gene_variant | MODIFIER | c.*4899G>A| |
S7 |