Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20990 | A06 | 11259583 | G | A | missense_variant | MODERATE | c.1463C>T|p.Ser488Leu |
S64 |
2 | BAA06g20990 | A06 | 11259718 | G | A | missense_variant | MODERATE | c.1328C>T|p.Thr443Ile |
S174 S216 S241 |
3 | BAA06g20990 | A06 | 11259921 | C | T | synonymous_variant | LOW | c.1125G>A|p.Arg375Arg |
S296 |
4 | BAA06g20990 | A06 | 11260101 | G | A | synonymous_variant | LOW | c.1026C>T|p.Asn342Asn |
S61 |
5 | BAA06g20990 | A06 | 11262281 | T | A | missense_variant | MODERATE | c.566A>T|p.Asn189Ile |
S199 |
6 | BAA06g20990 | A06 | 11262769 | G | A | synonymous_variant | LOW | c.78C>T|p.His26His |
S262 |
7 | BAA06g20990 | A06 | 11262878 | G | A | upstream_gene_variant | MODIFIER | c.-32C>T| |
S81 |
8 | BAA06g20990 | A06 | 11263002 | G | A | upstream_gene_variant | MODIFIER | c.-156C>T| |
S7 |
9 | BAA06g20990 | A06 | 11263464 | C | T | upstream_gene_variant | MODIFIER | c.-618G>A| |
S84 S93 |
10 | BAA06g20990 | A06 | 11267312 | G | A | upstream_gene_variant | MODIFIER | c.-4466C>T| |
S237 |
11 | BAA06g20990 | A06 | 11267325 | C | T | upstream_gene_variant | MODIFIER | c.-4479G>A| |
S15 S306 S308 |
12 | BAA06g20990 | A06 | 11267802 | G | A | upstream_gene_variant | MODIFIER | c.-4956C>T| |
S144 |