Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27900 | A10 | 21571796 | G | A | missense_variant | MODERATE | c.1417C>T|p.Leu473Phe |
S41 |
2 | BAA10g27900 | A10 | 21572040 | C | T | synonymous_variant | LOW | c.1173G>A|p.Lys391Lys |
S165 |
3 | BAA10g27900 | A10 | 21577031 | C | T | missense_variant | MODERATE | c.293G>A|p.Arg98His |
S87 |
4 | BAA10g27900 | A10 | 21577090 | G | A | synonymous_variant | LOW | c.234C>T|p.Gly78Gly |
S143 |
5 | BAA10g27900 | A10 | 21577390 | G | A | missense_variant | MODERATE | c.61C>T|p.Pro21Ser |
S217 S248 |
6 | BAA10g27900 | A10 | 21578824 | C | T | upstream_gene_variant | MODIFIER | c.-1285G>A| |
S282 |
7 | BAA10g27900 | A10 | 21578969 | G | A | upstream_gene_variant | MODIFIER | c.-1430C>T| |
S278 |
8 | BAA10g27900 | A10 | 21579034 | C | T | upstream_gene_variant | MODIFIER | c.-1495G>A| |
S33 |
9 | BAA10g27900 | A10 | 21580184 | C | T | upstream_gene_variant | MODIFIER | c.-2645G>A| |
S260 |
10 | BAA10g27900 | A10 | 21581978 | G | A | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S207 |