Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22800 | A07 | 26975165 | G | A | missense_variant | MODERATE | c.37G>A|p.Asp13Asn |
S15 S3 |
2 | BAA07g22800 | A07 | 26975540 | G | A | missense_variant | MODERATE | c.412G>A|p.Gly138Arg |
S87 |
3 | BAA07g22800 | A07 | 26976088 | G | A | synonymous_variant | LOW | c.960G>A|p.Leu320Leu |
S74 |
4 | BAA07g22800 | A07 | 26976089 | G | A | missense_variant | MODERATE | c.961G>A|p.Glu321Lys |
S39 |
5 | BAA07g22800 | A07 | 26976380 | G | A | missense_variant | MODERATE | c.1252G>A|p.Val418Ile |
S72 S78 |
6 | BAA07g22800 | A07 | 26976548 | G | A | missense_variant | MODERATE | c.1420G>A|p.Glu474Lys |
S125 |
7 | BAA07g22800 | A07 | 26976645 | G | A | missense_variant | MODERATE | c.1517G>A|p.Arg506His |
S208 S219 |
8 | BAA07g22800 | A07 | 26976684 | G | A | missense_variant | MODERATE | c.1556G>A|p.Gly519Asp |
S60 |
9 | BAA07g22800 | A07 | 26977261 | G | A | synonymous_variant | LOW | c.2133G>A|p.Arg711Arg |
S292 |
10 | BAA07g22800 | A07 | 26977272 | C | T | missense_variant | MODERATE | c.2144C>T|p.Ala715Val |
S35 |
11 | BAA07g22800 | A07 | 26977352 | C | T | synonymous_variant | LOW | c.2224C>T|p.Leu742Leu |
S236 |
12 | BAA07g22800 | A07 | 26980767 | G | A | downstream_gene_variant | MODIFIER | c.*3293G>A| |
S1 S90 |