Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08490 | A10 | 10257738 | C | T | upstream_gene_variant | MODIFIER | c.-3669C>T| |
S249 |
2 | BAA10g08490 | A10 | 10258011 | C | T | upstream_gene_variant | MODIFIER | c.-3396C>T| |
S177 |
3 | BAA10g08490 | A10 | 10258039 | G | A | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S129 |
4 | BAA10g08490 | A10 | 10258307 | C | T | upstream_gene_variant | MODIFIER | c.-3100C>T| |
S176 |
5 | BAA10g08490 | A10 | 10258709 | G | A | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S100 |
6 | BAA10g08490 | A10 | 10261871 | C | T | missense_variant | MODERATE | c.221C>T|p.Pro74Leu |
S208 S93 |
7 | BAA10g08490 | A10 | 10262574 | G | A | missense_variant | MODERATE | c.559G>A|p.Glu187Lys |
S138 |
8 | BAA10g08490 | A10 | 10262601 | G | T | stop_gained | HIGH | c.586G>T|p.Gly196* |
S9 |
9 | BAA10g08490 | A10 | 10265235 | C | T | downstream_gene_variant | MODIFIER | c.*2542C>T| |
S187 |
10 | BAA10g08490 | A10 | 10265512 | G | A | downstream_gene_variant | MODIFIER | c.*2819G>A| |
S207 |
11 | BAA10g08490 | A10 | 10265626 | C | T | downstream_gene_variant | MODIFIER | c.*2933C>T| |
S146 |
12 | BAA10g08490 | A10 | 10266559 | C | T | downstream_gene_variant | MODIFIER | c.*3866C>T| |
S249 |
13 | BAA10g08490 | A10 | 10266637 | C | T | downstream_gene_variant | MODIFIER | c.*3944C>T| |
S68 |
14 | BAA10g08490 | A10 | 10266670 | C | T | downstream_gene_variant | MODIFIER | c.*3977C>T| |
S169 |
15 | BAA10g08490 | A10 | 10267409 | G | A | downstream_gene_variant | MODIFIER | c.*4716G>A| |
S202 |