Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31370 | A01 | 20382153 | C | T | missense_variant | MODERATE | c.3952G>A|p.Glu1318Lys |
S167 |
2 | BAA01g31370 | A01 | 20382663 | C | T | missense_variant | MODERATE | c.3877G>A|p.Ala1293Thr |
S132 S137 S138 S215 S237 S288 S89 |
3 | BAA01g31370 | A01 | 20383441 | G | A | intron_variant | MODIFIER | c.3734+228C>T| |
S259 |
4 | BAA01g31370 | A01 | 20384085 | G | A | missense_variant | MODERATE | c.3538C>T|p.His1180Tyr |
S138 |
5 | BAA01g31370 | A01 | 20384901 | G | A | missense_variant | MODERATE | c.3305C>T|p.Thr1102Ile |
S45 |
6 | BAA01g31370 | A01 | 20385819 | C | T | missense_variant | MODERATE | c.2387G>A|p.Ser796Asn |
S277 |
7 | BAA01g31370 | A01 | 20385920 | G | A | synonymous_variant | LOW | c.2286C>T|p.Ala762Ala |
S280 |
8 | BAA01g31370 | A01 | 20386094 | C | T | synonymous_variant | LOW | c.2112G>A|p.Lys704Lys |
S50 |
9 | BAA01g31370 | A01 | 20386646 | G | A | synonymous_variant | LOW | c.1560C>T|p.Ser520Ser |
S280 |
10 | BAA01g31370 | A01 | 20387141 | C | T | synonymous_variant | LOW | c.1065G>A|p.Gly355Gly |
S1 S139 S90 |
11 | BAA01g31370 | A01 | 20387328 | C | T | missense_variant | MODERATE | c.878G>A|p.Arg293Lys |
S269 |
12 | BAA01g31370 | A01 | 20387572 | C | T | missense_variant | MODERATE | c.634G>A|p.Glu212Lys |
S180 |
13 | BAA01g31370 | A01 | 20387882 | C | T | synonymous_variant | LOW | c.324G>A|p.Lys108Lys |
S185 |
14 | BAA01g31370 | A01 | 20389059 | C | T | upstream_gene_variant | MODIFIER | c.-739G>A| |
S82 S92 |
15 | BAA01g31370 | A01 | 20389618 | C | T | upstream_gene_variant | MODIFIER | c.-1298G>A| |
S18 |
16 | BAA01g31370 | A01 | 20391375 | G | A | upstream_gene_variant | MODIFIER | c.-3055C>T| |
S84 S93 |
17 | BAA01g31370 | A01 | 20392944 | C | T | upstream_gene_variant | MODIFIER | c.-4624G>A| |
S81 S85 |