Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00920 | A10 | 424248 | G | A | missense_variant | MODERATE | c.3527C>T|p.Ala1176Val |
S245 |
2 | BAA10g00920 | A10 | 424344 | C | T | missense_variant | MODERATE | c.3431G>A|p.Arg1144Lys |
S182 |
3 | BAA10g00920 | A10 | 425729 | G | A | missense_variant | MODERATE | c.2360C>T|p.Pro787Leu |
S133 |
4 | BAA10g00920 | A10 | 425737 | G | A | synonymous_variant | LOW | c.2352C>T|p.Asp784Asp |
S186 |
5 | BAA10g00920 | A10 | 425834 | C | T | missense_variant | MODERATE | c.2255G>A|p.Arg752Lys |
S165 |
6 | BAA10g00920 | A10 | 426951 | C | T | missense_variant | MODERATE | c.1472G>A|p.Gly491Glu |
S275 |
7 | BAA10g00920 | A10 | 427473 | G | A | synonymous_variant | LOW | c.1041C>T|p.His347His |
S262 |
8 | BAA10g00920 | A10 | 427703 | C | T | missense_variant | MODERATE | c.811G>A|p.Val271Met |
S231 |
9 | BAA10g00920 | A10 | 427719 | G | A | synonymous_variant | LOW | c.795C>T|p.Val265Val |
S242 |
10 | BAA10g00920 | A10 | 428284 | G | A | missense_variant | MODERATE | c.230C>T|p.Pro77Leu |
S230 |
11 | BAA10g00920 | A10 | 428453 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S182 |
12 | BAA10g00920 | A10 | 429267 | C | T | upstream_gene_variant | MODIFIER | c.-754G>A| |
S10 S56 |
13 | BAA10g00920 | A10 | 430809 | C | T | upstream_gene_variant | MODIFIER | c.-2296G>A| |
S180 |
14 | BAA10g00920 | A10 | 433246 | C | T | upstream_gene_variant | MODIFIER | c.-4733G>A| |
S135 |