Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08850 | A04 | 6125903 | G | A | upstream_gene_variant | MODIFIER | c.-4427G>A| |
S71 |
2 | BAA04g08850 | A04 | 6126111 | C | T | upstream_gene_variant | MODIFIER | c.-4219C>T| |
S255 |
3 | BAA04g08850 | A04 | 6127164 | C | T | upstream_gene_variant | MODIFIER | c.-3166C>T| |
S260 |
4 | BAA04g08850 | A04 | 6127571 | C | T | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S20 |
5 | BAA04g08850 | A04 | 6127875 | G | A | upstream_gene_variant | MODIFIER | c.-2455G>A| |
S54 |
6 | BAA04g08850 | A04 | 6128332 | C | T | upstream_gene_variant | MODIFIER | c.-1998C>T| |
S173 |
7 | BAA04g08850 | A04 | 6129485 | C | T | upstream_gene_variant | MODIFIER | c.-845C>T| |
S283 |
8 | BAA04g08850 | A04 | 6130322 | G | A | upstream_gene_variant | MODIFIER | c.-8G>A| |
S133 |
9 | BAA04g08850 | A04 | 6131528 | G | A | stop_gained&splice_region_variant | HIGH | c.786G>A|p.Trp262* |
S153 S213 |
10 | BAA04g08850 | A04 | 6132124 | C | T | missense_variant | MODERATE | c.1108C>T|p.Leu370Phe |
S92 |
11 | BAA04g08850 | A04 | 6132142 | C | T | splice_region_variant&intron_variant | LOW | c.1118+8C>T| |
S76 |
12 | BAA04g08850 | A04 | 6132267 | G | A | missense_variant | MODERATE | c.1162G>A|p.Glu388Lys |
S303 |
13 | BAA04g08850 | A04 | 6132529 | G | A | missense_variant | MODERATE | c.1339G>A|p.Asp447Asn |
S103 |
14 | BAA04g08850 | A04 | 6132573 | G | A | synonymous_variant | LOW | c.1383G>A|p.Leu461Leu |
S176 |
15 | BAA04g08850 | A04 | 6132605 | C | T | missense_variant | MODERATE | c.1415C>T|p.Thr472Ile |
S196 |
16 | BAA04g08850 | A04 | 6135510 | G | A | downstream_gene_variant | MODIFIER | c.*2820G>A| |
S5 |