Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05470 | A10 | 2794281 | G | A | missense_variant | MODERATE | c.1246C>T|p.Pro416Ser |
S251 |
2 | BAA10g05470 | A10 | 2795001 | C | T | missense_variant | MODERATE | c.526G>A|p.Asp176Asn |
S10 |
3 | BAA10g05470 | A10 | 2795480 | G | A | missense_variant | MODERATE | c.47C>T|p.Ser16Phe |
S262 |
4 | BAA10g05470 | A10 | 2795613 | G | A | upstream_gene_variant | MODIFIER | c.-87C>T| |
S219 S72 |
5 | BAA10g05470 | A10 | 2796008 | G | A | upstream_gene_variant | MODIFIER | c.-482C>T| |
S215 |
6 | BAA10g05470 | A10 | 2796024 | C | T | upstream_gene_variant | MODIFIER | c.-498G>A| |
S286 |
7 | BAA10g05470 | A10 | 2796416 | G | A | upstream_gene_variant | MODIFIER | c.-890C>T| |
S221 |
8 | BAA10g05470 | A10 | 2796631 | C | T | upstream_gene_variant | MODIFIER | c.-1105G>A| |
S200 |
9 | BAA10g05470 | A10 | 2797184 | G | A | upstream_gene_variant | MODIFIER | c.-1658C>T| |
S120 |
10 | BAA10g05470 | A10 | 2799062 | G | A | upstream_gene_variant | MODIFIER | c.-3536C>T| |
S50 |
11 | BAA10g05470 | A10 | 2799411 | C | T | upstream_gene_variant | MODIFIER | c.-3885G>A| |
S132 S137 S89 |
12 | BAA10g05470 | A10 | 2799658 | C | T | upstream_gene_variant | MODIFIER | c.-4132G>A| |
S235 |
13 | BAA10g05470 | A10 | 2799813 | C | T | upstream_gene_variant | MODIFIER | c.-4287G>A| |
S35 |
14 | BAA10g05470 | A10 | 2799995 | C | T | upstream_gene_variant | MODIFIER | c.-4469G>A| |
S282 |