Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02680 | A01 | 1224877 | C | T | synonymous_variant | LOW | c.441C>T|p.Asn147Asn |
S18 |
2 | BAA01g02680 | A01 | 1225242 | G | A | missense_variant | MODERATE | c.731G>A|p.Gly244Glu |
S228 |
3 | BAA01g02680 | A01 | 1225359 | C | T | missense_variant | MODERATE | c.848C>T|p.Thr283Met |
S35 |
4 | BAA01g02680 | A01 | 1225476 | C | T | missense_variant | MODERATE | c.965C>T|p.Ser322Phe |
S125 |
5 | BAA01g02680 | A01 | 1225855 | G | A | synonymous_variant | LOW | c.1344G>A|p.Glu448Glu |
S56 |
6 | BAA01g02680 | A01 | 1226436 | C | T | missense_variant | MODERATE | c.1925C>T|p.Ser642Leu |
S81 S85 |
7 | BAA01g02680 | A01 | 1226740 | G | A | synonymous_variant | LOW | c.2229G>A|p.Arg743Arg |
S296 S89 |
8 | BAA01g02680 | A01 | 1227340 | G | A | synonymous_variant | LOW | c.2829G>A|p.Gly943Gly |
S37 |
9 | BAA01g02680 | A01 | 1229435 | C | T | downstream_gene_variant | MODIFIER | c.*1116C>T| |
S151 |
10 | BAA01g02680 | A01 | 1229669 | C | T | downstream_gene_variant | MODIFIER | c.*1350C>T| |
S130 |
11 | BAA01g02680 | A01 | 1230190 | C | T | downstream_gene_variant | MODIFIER | c.*1871C>T| |
S139 |
12 | BAA01g02680 | A01 | 1231486 | C | T | downstream_gene_variant | MODIFIER | c.*3167C>T| |
S230 |
13 | BAA01g02680 | A01 | 1233155 | C | T | downstream_gene_variant | MODIFIER | c.*4836C>T| |
S202 |