Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17680 | A10 | 16898382 | C | T | missense_variant | MODERATE | c.2251G>A|p.Asp751Asn |
S283 |
2 | BAA10g17680 | A10 | 16898540 | C | A | missense_variant | MODERATE | c.2093G>T|p.Gly698Val |
S96 |
3 | BAA10g17680 | A10 | 16898634 | C | T | missense_variant | MODERATE | c.1999G>A|p.Glu667Lys |
S148 S210 S30 S31 |
4 | BAA10g17680 | A10 | 16899053 | T | A | missense_variant | MODERATE | c.1580A>T|p.Glu527Val |
S281 |
5 | BAA10g17680 | A10 | 16899113 | G | A | missense_variant | MODERATE | c.1520C>T|p.Thr507Met |
S159 S243 |
6 | BAA10g17680 | A10 | 16900518 | C | T | missense_variant | MODERATE | c.115G>A|p.Val39Ile |
S117 |
7 | BAA10g17680 | A10 | 16901837 | G | A | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S241 |
8 | BAA10g17680 | A10 | 16902399 | G | A | upstream_gene_variant | MODIFIER | c.-1767C>T| |
S9 |
9 | BAA10g17680 | A10 | 16902612 | C | T | upstream_gene_variant | MODIFIER | c.-1980G>A| |
S70 |
10 | BAA10g17680 | A10 | 16902896 | C | T | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S130 |
11 | BAA10g17680 | A10 | 16904770 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S239 |
12 | BAA10g17680 | A10 | 16905196 | G | A | upstream_gene_variant | MODIFIER | c.-4564C>T| |
S138 |
13 | BAA10g17680 | A10 | 16905389 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S203 |