Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g28100 | A07 | 29473552 | C | T | missense_variant | MODERATE | c.2953G>A|p.Asp985Asn |
S126 |
2 | BAA07g28100 | A07 | 29473679 | G | A | synonymous_variant | LOW | c.2826C>T|p.Ser942Ser |
S38 |
3 | BAA07g28100 | A07 | 29474014 | C | T | missense_variant | MODERATE | c.2491G>A|p.Asp831Asn |
S293 |
4 | BAA07g28100 | A07 | 29474221 | C | T | missense_variant | MODERATE | c.2284G>A|p.Glu762Lys |
S288 |
5 | BAA07g28100 | A07 | 29474441 | G | A | synonymous_variant | LOW | c.2064C>T|p.His688His |
S257 |
6 | BAA07g28100 | A07 | 29474460 | C | T | missense_variant | MODERATE | c.2045G>A|p.Ser682Asn |
S301 S304 |
7 | BAA07g28100 | A07 | 29474654 | C | T | synonymous_variant | LOW | c.1851G>A|p.Ala617Ala |
S221 |
8 | BAA07g28100 | A07 | 29475241 | G | A | stop_gained | HIGH | c.1264C>T|p.Gln422* |
S1 S90 |
9 | BAA07g28100 | A07 | 29475406 | C | T | missense_variant | MODERATE | c.1099G>A|p.Asp367Asn |
S221 |
10 | BAA07g28100 | A07 | 29475440 | C | T | stop_gained | HIGH | c.1065G>A|p.Trp355* |
S127 |
11 | BAA07g28100 | A07 | 29476277 | C | T | synonymous_variant | LOW | c.228G>A|p.Gln76Gln |
S71 |
12 | BAA07g28100 | A07 | 29476509 | G | A | upstream_gene_variant | MODIFIER | c.-5C>T| |
S268 |
13 | BAA07g28100 | A07 | 29478146 | G | A | upstream_gene_variant | MODIFIER | c.-1642C>T| |
S115 |
14 | BAA07g28100 | A07 | 29479310 | C | T | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S218 |
15 | BAA07g28100 | A07 | 29479829 | C | T | upstream_gene_variant | MODIFIER | c.-3325G>A| |
S302 |
16 | BAA07g28100 | A07 | 29480011 | G | A | upstream_gene_variant | MODIFIER | c.-3507C>T| |
S240 |
17 | BAA07g28100 | A07 | 29480085 | G | A | upstream_gene_variant | MODIFIER | c.-3581C>T| |
S282 |
18 | BAA07g28100 | A07 | 29480087 | G | A | upstream_gene_variant | MODIFIER | c.-3583C>T| |
S295 |