Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28130 | A10 | 21671750 | C | T | upstream_gene_variant | MODIFIER | c.-1956C>T| |
S146 |
2 | BAA10g28130 | A10 | 21672140 | G | A | upstream_gene_variant | MODIFIER | c.-1566G>A| |
S262 |
3 | BAA10g28130 | A10 | 21672551 | C | T | upstream_gene_variant | MODIFIER | c.-1155C>T| |
S135 |
4 | BAA10g28130 | A10 | 21672929 | G | A | upstream_gene_variant | MODIFIER | c.-777G>A| |
S95 |
5 | BAA10g28130 | A10 | 21673241 | G | A | upstream_gene_variant | MODIFIER | c.-465G>A| |
S63 |
6 | BAA10g28130 | A10 | 21673787 | C | T | missense_variant | MODERATE | c.82C>T|p.Pro28Ser |
S308 |
7 | BAA10g28130 | A10 | 21673913 | C | T | missense_variant | MODERATE | c.208C>T|p.Leu70Phe |
S121 |
8 | BAA10g28130 | A10 | 21674322 | C | T | intron_variant | MODIFIER | c.414+16C>T| |
S247 |
9 | BAA10g28130 | A10 | 21674391 | G | A | missense_variant | MODERATE | c.422G>A|p.Gly141Glu |
S202 |