Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39920 | A01 | 26515141 | C | T | missense_variant | MODERATE | c.1810G>A|p.Gly604Arg |
S120 |
2 | BAA01g39920 | A01 | 26515476 | G | A | missense_variant | MODERATE | c.1475C>T|p.Ser492Phe |
S105 |
3 | BAA01g39920 | A01 | 26515532 | C | T | synonymous_variant | LOW | c.1419G>A|p.Gln473Gln |
S303 |
4 | BAA01g39920 | A01 | 26515772 | G | A | missense_variant | MODERATE | c.1271C>T|p.Ser424Phe |
S45 |
5 | BAA01g39920 | A01 | 26516088 | G | A | missense_variant | MODERATE | c.1123C>T|p.His375Tyr |
S160 |
6 | BAA01g39920 | A01 | 26518011 | C | T | missense_variant | MODERATE | c.364G>A|p.Gly122Ser |
S48 |
7 | BAA01g39920 | A01 | 26520016 | C | T | intron_variant | MODIFIER | c.46-1349G>A| |
S134 |
8 | BAA01g39920 | A01 | 26520899 | C | T | intron_variant | MODIFIER | c.46-2232G>A| |
S182 |
9 | BAA01g39920 | A01 | 26523066 | G | A | intron_variant | MODIFIER | c.46-4399C>T| |
S281 |
10 | BAA01g39920 | A01 | 26523125 | C | T | intron_variant | MODIFIER | c.46-4458G>A| |
S293 |
11 | BAA01g39920 | A01 | 26523775 | G | A | intron_variant | MODIFIER | c.45+3942C>T| |
S71 |
12 | BAA01g39920 | A01 | 26524477 | C | T | intron_variant | MODIFIER | c.45+3240G>A| |
S289 S290 |
13 | BAA01g39920 | A01 | 26528682 | C | T | upstream_gene_variant | MODIFIER | c.-921G>A| |
S88 |