Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07510 | A08 | 6779723 | G | A | missense_variant | MODERATE | c.352G>A|p.Asp118Asn |
S221 |
2 | BAA08g07510 | A08 | 6779781 | C | T | missense_variant | MODERATE | c.410C>T|p.Pro137Leu |
S233 |
3 | BAA08g07510 | A08 | 6779903 | C | T | missense_variant | MODERATE | c.532C>T|p.Pro178Ser |
S261 |
4 | BAA08g07510 | A08 | 6780491 | C | T | missense_variant | MODERATE | c.1120C>T|p.Pro374Ser |
S152 |
5 | BAA08g07510 | A08 | 6780525 | G | A | missense_variant | MODERATE | c.1154G>A|p.Arg385His |
S20 |
6 | BAA08g07510 | A08 | 6780545 | C | T | missense_variant | MODERATE | c.1174C>T|p.Pro392Ser |
S70 |
7 | BAA08g07510 | A08 | 6780688 | G | A | synonymous_variant | LOW | c.1317G>A|p.Gly439Gly |
S131 |
8 | BAA08g07510 | A08 | 6781516 | G | A | missense_variant | MODERATE | c.1738G>A|p.Ala580Thr |
S115 |
9 | BAA08g07510 | A08 | 6781569 | C | T | synonymous_variant | LOW | c.1791C>T|p.Phe597Phe |
S60 |
10 | BAA08g07510 | A08 | 6781585 | G | A | missense_variant | MODERATE | c.1807G>A|p.Ala603Thr |
S139 |
11 | BAA08g07510 | A08 | 6781913 | C | T | missense_variant | MODERATE | c.2135C>T|p.Ser712Phe |
S174 S216 S241 |
12 | BAA08g07510 | A08 | 6782259 | C | T | synonymous_variant | LOW | c.2481C>T|p.Arg827Arg |
S143 |
13 | BAA08g07510 | A08 | 6782439 | C | T | synonymous_variant | LOW | c.2571C>T|p.Cys857Cys |
S47 |
14 | BAA08g07510 | A08 | 6782473 | G | A | missense_variant | MODERATE | c.2605G>A|p.Val869Met |
S262 |
15 | BAA08g07510 | A08 | 6785524 | C | T | downstream_gene_variant | MODIFIER | c.*3040C>T| |
S15 S156 S3 S34 S6 |
16 | BAA08g07510 | A08 | 6785604 | G | A | downstream_gene_variant | MODIFIER | c.*3120G>A| |
S238 |