Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09890 | A10 | 11726486 | G | A | missense_variant | MODERATE | c.4G>A|p.Val2Met |
S290 |
2 | BAA10g09890 | A10 | 11726528 | C | T | missense_variant | MODERATE | c.46C>T|p.Pro16Ser |
S162 |
3 | BAA10g09890 | A10 | 11726570 | C | T | missense_variant | MODERATE | c.88C>T|p.Arg30Cys |
S247 |
4 | BAA10g09890 | A10 | 11726684 | G | A | missense_variant | MODERATE | c.202G>A|p.Gly68Arg |
S262 |
5 | BAA10g09890 | A10 | 11727137 | C | T | intron_variant | MODIFIER | c.242-76C>T| |
S246 |
6 | BAA10g09890 | A10 | 11727252 | C | T | missense_variant | MODERATE | c.281C>T|p.Pro94Leu |
S208 S93 |
7 | BAA10g09890 | A10 | 11727295 | C | T | synonymous_variant | LOW | c.324C>T|p.His108His |
S269 |
8 | BAA10g09890 | A10 | 11727362 | G | A | missense_variant | MODERATE | c.391G>A|p.Asp131Asn |
S65 |
9 | BAA10g09890 | A10 | 11727453 | G | A | intron_variant | MODIFIER | c.433-45G>A| |
S75 S81 |
10 | BAA10g09890 | A10 | 11728160 | G | A | downstream_gene_variant | MODIFIER | c.*354G>A| |
S302 |
11 | BAA10g09890 | A10 | 11728513 | C | T | downstream_gene_variant | MODIFIER | c.*707C>T| |
S70 |
12 | BAA10g09890 | A10 | 11728843 | C | T | downstream_gene_variant | MODIFIER | c.*1037C>T| |
S146 |
13 | BAA10g09890 | A10 | 11729395 | C | T | downstream_gene_variant | MODIFIER | c.*1589C>T| |
S149 |
14 | BAA10g09890 | A10 | 11730006 | C | T | downstream_gene_variant | MODIFIER | c.*2200C>T| |
S23 |
15 | BAA10g09890 | A10 | 11730705 | G | A | downstream_gene_variant | MODIFIER | c.*2899G>A| |
S202 |
16 | BAA10g09890 | A10 | 11731090 | G | A | downstream_gene_variant | MODIFIER | c.*3284G>A| |
S172 S217 |
17 | BAA10g09890 | A10 | 11731672 | C | T | downstream_gene_variant | MODIFIER | c.*3866C>T| |
S167 |
18 | BAA10g09890 | A10 | 11732190 | C | T | downstream_gene_variant | MODIFIER | c.*4384C>T| |
S176 |
19 | BAA10g09890 | A10 | 11732276 | G | A | downstream_gene_variant | MODIFIER | c.*4470G>A| |
S292 |
20 | BAA10g09890 | A10 | 11732489 | C | T | downstream_gene_variant | MODIFIER | c.*4683C>T| |
S80 |
21 | BAA10g09890 | A10 | 11732690 | C | T | downstream_gene_variant | MODIFIER | c.*4884C>T| |
S116 |