Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07730 | A10 | 4702144 | G | A | missense_variant | MODERATE | c.508G>A|p.Asp170Asn |
S268 |
2 | BAA10g07730 | A10 | 4702243 | G | A | missense_variant | MODERATE | c.607G>A|p.Ala203Thr |
S192 |
3 | BAA10g07730 | A10 | 4702675 | C | T | missense_variant | MODERATE | c.919C>T|p.Leu307Phe |
S97 |
4 | BAA10g07730 | A10 | 4703258 | G | A | missense_variant | MODERATE | c.1502G>A|p.Ser501Asn |
S78 |
5 | BAA10g07730 | A10 | 4704440 | C | T | missense_variant | MODERATE | c.2246C>T|p.Pro749Leu |
S165 |
6 | BAA10g07730 | A10 | 4704722 | G | A | missense_variant | MODERATE | c.2528G>A|p.Gly843Glu |
S19 |
7 | BAA10g07730 | A10 | 4704774 | G | A | synonymous_variant | LOW | c.2580G>A|p.Ala860Ala |
S164 |
8 | BAA10g07730 | A10 | 4704846 | G | A | synonymous_variant | LOW | c.2652G>A|p.Lys884Lys |
S68 |
9 | BAA10g07730 | A10 | 4706380 | C | T | downstream_gene_variant | MODIFIER | c.*1522C>T| |
S155 S211 |
10 | BAA10g07730 | A10 | 4706778 | G | A | downstream_gene_variant | MODIFIER | c.*1920G>A| |
S292 |
11 | BAA10g07730 | A10 | 4708839 | G | A | downstream_gene_variant | MODIFIER | c.*3981G>A| |
S289 |
12 | BAA10g07730 | A10 | 4709152 | A | G | downstream_gene_variant | MODIFIER | c.*4294A>G| |
S159 S243 |
13 | BAA10g07730 | A10 | 4709658 | C | T | downstream_gene_variant | MODIFIER | c.*4800C>T| |
S63 |