Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12170 | A10 | 13629917 | C | T | missense_variant | MODERATE | c.2285G>A|p.Arg762Lys |
S196 |
2 | BAA10g12170 | A10 | 13630014 | C | T | missense_variant | MODERATE | c.2188G>A|p.Gly730Ser |
S203 |
3 | BAA10g12170 | A10 | 13632226 | G | A | synonymous_variant | LOW | c.837C>T|p.Asn279Asn |
S271 |
4 | BAA10g12170 | A10 | 13632912 | C | T | missense_variant | MODERATE | c.151G>A|p.Asp51Asn |
S20 |
5 | BAA10g12170 | A10 | 13632942 | C | T | missense_variant | MODERATE | c.121G>A|p.Asp41Asn |
S282 |
6 | BAA10g12170 | A10 | 13632950 | G | A | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S202 |
7 | BAA10g12170 | A10 | 13634297 | C | T | upstream_gene_variant | MODIFIER | c.-1235G>A| |
S210 S225 |
8 | BAA10g12170 | A10 | 13635999 | C | T | upstream_gene_variant | MODIFIER | c.-2937G>A| |
S190 |
9 | BAA10g12170 | A10 | 13636022 | G | A | upstream_gene_variant | MODIFIER | c.-2960C>T| |
S151 S257 S263 |
10 | BAA10g12170 | A10 | 13637043 | C | T | upstream_gene_variant | MODIFIER | c.-3981G>A| |
S305 |
11 | BAA10g12170 | A10 | 13637511 | G | A | upstream_gene_variant | MODIFIER | c.-4449C>T| |
S228 |
12 | BAA10g12170 | A10 | 13637752 | G | A | upstream_gene_variant | MODIFIER | c.-4690C>T| |
S171 |
13 | BAA10g12170 | A10 | 13637958 | G | A | upstream_gene_variant | MODIFIER | c.-4896C>T| |
S192 |