Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26010 | A05 | 30719647 | G | A | synonymous_variant | LOW | c.2289C>T|p.Asn763Asn |
S192 |
2 | BAA05g26010 | A05 | 30719880 | C | T | missense_variant | MODERATE | c.2056G>A|p.Asp686Asn |
S177 |
3 | BAA05g26010 | A05 | 30720183 | C | T | missense_variant | MODERATE | c.1753G>A|p.Glu585Lys |
S288 |
4 | BAA05g26010 | A05 | 30720963 | C | T | intron_variant | MODIFIER | c.1226+58G>A| |
S108 |
5 | BAA05g26010 | A05 | 30721658 | C | T | missense_variant | MODERATE | c.761G>A|p.Gly254Glu |
S193 |
6 | BAA05g26010 | A05 | 30721897 | G | A | intron_variant | MODIFIER | c.677-24C>T| |
S176 |
7 | BAA05g26010 | A05 | 30722672 | C | T | synonymous_variant | LOW | c.576G>A|p.Lys192Lys |
S130 |
8 | BAA05g26010 | A05 | 30722764 | C | T | missense_variant | MODERATE | c.484G>A|p.Asp162Asn |
S88 |
9 | BAA05g26010 | A05 | 30722937 | C | T | intron_variant | MODIFIER | c.391-80G>A| |
S255 |
10 | BAA05g26010 | A05 | 30723093 | G | A | intron_variant | MODIFIER | c.391-236C>T| |
S216 S265 |
11 | BAA05g26010 | A05 | 30723376 | A | G | intron_variant | MODIFIER | c.390+14T>C| |
S182 |
12 | BAA05g26010 | A05 | 30724608 | G | A | upstream_gene_variant | MODIFIER | c.-829C>T| |
S296 |
13 | BAA05g26010 | A05 | 30725277 | C | T | upstream_gene_variant | MODIFIER | c.-1498G>A| |
S241 |
14 | BAA05g26010 | A05 | 30725838 | G | A | upstream_gene_variant | MODIFIER | c.-2059C>T| |
S276 |
15 | BAA05g26010 | A05 | 30726973 | G | A | upstream_gene_variant | MODIFIER | c.-3194C>T| |
S168 |