Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g04090 | A06 | 2267862 | C | T | missense_variant | MODERATE | c.2665G>A|p.Asp889Asn |
S259 |
2 | BAA06g04090 | A06 | 2272334 | G | A | synonymous_variant | LOW | c.1536C>T|p.Asp512Asp |
S219 S72 |
3 | BAA06g04090 | A06 | 2272474 | C | T | missense_variant | MODERATE | c.1396G>A|p.Asp466Asn |
S209 |
4 | BAA06g04090 | A06 | 2272479 | G | A | missense_variant | MODERATE | c.1391C>T|p.Ser464Phe |
S8 |
5 | BAA06g04090 | A06 | 2272556 | C | T | synonymous_variant | LOW | c.1314G>A|p.Gln438Gln |
S124 |
6 | BAA06g04090 | A06 | 2272829 | C | T | synonymous_variant | LOW | c.1041G>A|p.Gln347Gln |
S7 |
7 | BAA06g04090 | A06 | 2273717 | G | A | intron_variant | MODIFIER | c.278-125C>T| |
S45 |
8 | BAA06g04090 | A06 | 2273722 | C | T | intron_variant | MODIFIER | c.278-130G>A| |
S262 |
9 | BAA06g04090 | A06 | 2274412 | C | T | upstream_gene_variant | MODIFIER | c.-274G>A| |
S225 S73 |
10 | BAA06g04090 | A06 | 2275974 | C | T | upstream_gene_variant | MODIFIER | c.-1836G>A| |
S76 |
11 | BAA06g04090 | A06 | 2277489 | C | T | upstream_gene_variant | MODIFIER | c.-3351G>A| |
S279 |
12 | BAA06g04090 | A06 | 2277814 | G | A | upstream_gene_variant | MODIFIER | c.-3676C>T| |
S278 |