Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g35540 | A06 | 23717602 | C | T | missense_variant | MODERATE | c.121C>T|p.Arg41Cys |
S95 |
2 | BAA06g35540 | A06 | 23717623 | C | T | missense_variant | MODERATE | c.142C>T|p.Pro48Ser |
S262 |
3 | BAA06g35540 | A06 | 23718550 | C | T | synonymous_variant | LOW | c.228C>T|p.Asn76Asn |
S172 S217 |
4 | BAA06g35540 | A06 | 23718771 | G | A | missense_variant | MODERATE | c.449G>A|p.Gly150Glu |
S78 S83 |
5 | BAA06g35540 | A06 | 23718809 | G | A | intron_variant | MODIFIER | c.460+27G>A| |
S37 |
6 | BAA06g35540 | A06 | 23718810 | G | A | intron_variant | MODIFIER | c.460+28G>A| |
S208 S219 |
7 | BAA06g35540 | A06 | 23718965 | C | T | intron_variant | MODIFIER | c.460+183C>T| |
S58 |
8 | BAA06g35540 | A06 | 23719359 | C | T | synonymous_variant | LOW | c.534C>T|p.Tyr178Tyr |
S40 S49 |
9 | BAA06g35540 | A06 | 23719389 | G | A | intron_variant | MODIFIER | c.542+22G>A| |
S175 |
10 | BAA06g35540 | A06 | 23719621 | G | A | intron_variant | MODIFIER | c.654+62G>A| |
S117 |
11 | BAA06g35540 | A06 | 23719627 | G | A | intron_variant | MODIFIER | c.654+68G>A| |
S39 |
12 | BAA06g35540 | A06 | 23720325 | C | T | missense_variant | MODERATE | c.899C>T|p.Ala300Val |
S105 S106 |
13 | BAA06g35540 | A06 | 23721162 | C | T | downstream_gene_variant | MODIFIER | c.*785C>T| |
S108 |
14 | BAA06g35540 | A06 | 23721916 | C | T | downstream_gene_variant | MODIFIER | c.*1539C>T| |
S43 |
15 | BAA06g35540 | A06 | 23723917 | G | A | downstream_gene_variant | MODIFIER | c.*3540G>A| |
S173 |
16 | BAA06g35540 | A06 | 23724581 | G | A | downstream_gene_variant | MODIFIER | c.*4204G>A| |
S201 |
17 | BAA06g35540 | A06 | 23725296 | T | G | downstream_gene_variant | MODIFIER | c.*4919T>G| |
S283 S303 |