Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05560 | A01 | 2444298 | C | T | upstream_gene_variant | MODIFIER | c.-3887C>T| |
S53 |
2 | BAA01g05560 | A01 | 2444534 | G | A | upstream_gene_variant | MODIFIER | c.-3651G>A| |
S107 |
3 | BAA01g05560 | A01 | 2444713 | G | A | upstream_gene_variant | MODIFIER | c.-3472G>A| |
S95 |
4 | BAA01g05560 | A01 | 2445098 | G | A | upstream_gene_variant | MODIFIER | c.-3087G>A| |
S289 S290 |
5 | BAA01g05560 | A01 | 2446090 | G | A | upstream_gene_variant | MODIFIER | c.-2095G>A| |
S242 |
6 | BAA01g05560 | A01 | 2447559 | G | A | upstream_gene_variant | MODIFIER | c.-626G>A| |
S117 S40 S49 |
7 | BAA01g05560 | A01 | 2448373 | G | A | stop_gained | HIGH | c.189G>A|p.Trp63* |
S157 |
8 | BAA01g05560 | A01 | 2449090 | C | T | intron_variant | MODIFIER | c.468-19C>T| |
S67 |
9 | BAA01g05560 | A01 | 2449838 | G | A | missense_variant | MODERATE | c.938G>A|p.Ser313Asn |
S87 |
10 | BAA01g05560 | A01 | 2449903 | C | T | missense_variant | MODERATE | c.1003C>T|p.Leu335Phe |
S18 |
11 | BAA01g05560 | A01 | 2451592 | G | A | missense_variant | MODERATE | c.1867G>A|p.Gly623Arg |
S12 |
12 | BAA01g05560 | A01 | 2451830 | G | A | missense_variant | MODERATE | c.2105G>A|p.Arg702Lys |
S23 |
13 | BAA01g05560 | A01 | 2453041 | C | T | downstream_gene_variant | MODIFIER | c.*424C>T| |
S291 |
14 | BAA01g05560 | A01 | 2453167 | G | A | downstream_gene_variant | MODIFIER | c.*550G>A| |
S224 |
15 | BAA01g05560 | A01 | 2454877 | G | A | downstream_gene_variant | MODIFIER | c.*2260G>A| |
S153 S213 S34 |
16 | BAA01g05560 | A01 | 2455160 | G | A | downstream_gene_variant | MODIFIER | c.*2543G>A| |
S274 |