Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27090 | A10 | 21208409 | C | T | missense_variant | MODERATE | c.1244G>A|p.Gly415Asp |
S128 S301 S304 |
2 | BAA10g27090 | A10 | 21208855 | G | A | missense_variant | MODERATE | c.971C>T|p.Ser324Phe |
S174 S27 |
3 | BAA10g27090 | A10 | 21208942 | G | A | missense_variant | MODERATE | c.884C>T|p.Ser295Phe |
S179 |
4 | BAA10g27090 | A10 | 21208969 | G | A | missense_variant | MODERATE | c.857C>T|p.Ala286Val |
S143 |
5 | BAA10g27090 | A10 | 21209017 | G | A | splice_region_variant&intron_variant | LOW | c.815-6C>T| |
S66 |
6 | BAA10g27090 | A10 | 21211570 | C | T | upstream_gene_variant | MODIFIER | c.-626G>A| |
S306 S308 |
7 | BAA10g27090 | A10 | 21211817 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| |
S119 |
8 | BAA10g27090 | A10 | 21212276 | G | A | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S181 |
9 | BAA10g27090 | A10 | 21214651 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S99 |
10 | BAA10g27090 | A10 | 21215550 | C | T | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S10 |
11 | BAA10g27090 | A10 | 21215709 | G | A | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S245 |