Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g32660 | A07 | 32013432 | C | T | missense_variant | MODERATE | c.2104G>A|p.Asp702Asn |
S265 |
2 | BAA07g32660 | A07 | 32013438 | C | T | missense_variant | MODERATE | c.2098G>A|p.Ala700Thr |
S237 |
3 | BAA07g32660 | A07 | 32014162 | C | T | missense_variant | MODERATE | c.1978G>A|p.Asp660Asn |
S237 |
4 | BAA07g32660 | A07 | 32014333 | C | T | missense_variant | MODERATE | c.1807G>A|p.Glu603Lys |
S245 |
5 | BAA07g32660 | A07 | 32014444 | G | A | stop_gained | HIGH | c.1696C>T|p.Gln566* |
S18 |
6 | BAA07g32660 | A07 | 32014549 | G | A | missense_variant | MODERATE | c.1591C>T|p.Leu531Phe |
S69 |
7 | BAA07g32660 | A07 | 32014642 | G | A | missense_variant | MODERATE | c.1498C>T|p.Pro500Ser |
S130 |
8 | BAA07g32660 | A07 | 32016071 | G | A | missense_variant | MODERATE | c.436C>T|p.Pro146Ser |
S125 |
9 | BAA07g32660 | A07 | 32016355 | C | T | synonymous_variant | LOW | c.315G>A|p.Gln105Gln |
S232 |
10 | BAA07g32660 | A07 | 32017267 | G | A | upstream_gene_variant | MODIFIER | c.-323C>T| |
S130 |
11 | BAA07g32660 | A07 | 32019435 | C | T | upstream_gene_variant | MODIFIER | c.-2491G>A| |
S203 |
12 | BAA07g32660 | A07 | 32019602 | G | A | upstream_gene_variant | MODIFIER | c.-2658C>T| |
S70 |
13 | BAA07g32660 | A07 | 32021223 | G | A | upstream_gene_variant | MODIFIER | c.-4279C>T| |
S302 |