Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03590 | A10 | 1728210 | G | A | missense_variant | MODERATE | c.1385C>T|p.Pro462Leu |
S43 |
2 | BAA10g03590 | A10 | 1728664 | G | A | missense_variant | MODERATE | c.931C>T|p.Leu311Phe |
S13 |
3 | BAA10g03590 | A10 | 1729305 | G | A | missense_variant | MODERATE | c.290C>T|p.Ala97Val |
S211 S227 |
4 | BAA10g03590 | A10 | 1729363 | C | T | missense_variant | MODERATE | c.232G>A|p.Asp78Asn |
S121 |
5 | BAA10g03590 | A10 | 1729459 | G | A | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S150 |
6 | BAA10g03590 | A10 | 1732103 | G | A | upstream_gene_variant | MODIFIER | c.-2509C>T| |
S282 |
7 | BAA10g03590 | A10 | 1732106 | G | A | upstream_gene_variant | MODIFIER | c.-2512C>T| |
S284 |
8 | BAA10g03590 | A10 | 1732639 | C | T | upstream_gene_variant | MODIFIER | c.-3045G>A| |
S206 S26 |
9 | BAA10g03590 | A10 | 1733549 | G | A | upstream_gene_variant | MODIFIER | c.-3955C>T| |
S295 |
10 | BAA10g03590 | A10 | 1733947 | G | A | upstream_gene_variant | MODIFIER | c.-4353C>T| |
S274 |