Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04750 | A10 | 2432327 | C | T | upstream_gene_variant | MODIFIER | c.-4751C>T| |
S238 |
2 | BAA10g04750 | A10 | 2432649 | G | A | upstream_gene_variant | MODIFIER | c.-4429G>A| |
S112 |
3 | BAA10g04750 | A10 | 2432665 | G | A | upstream_gene_variant | MODIFIER | c.-4413G>A| |
S48 |
4 | BAA10g04750 | A10 | 2432890 | C | T | upstream_gene_variant | MODIFIER | c.-4188C>T| |
S146 |
5 | BAA10g04750 | A10 | 2433917 | G | A | upstream_gene_variant | MODIFIER | c.-3161G>A| |
S262 |
6 | BAA10g04750 | A10 | 2433978 | G | A | upstream_gene_variant | MODIFIER | c.-3100G>A| |
S156 |
7 | BAA10g04750 | A10 | 2434837 | G | A | upstream_gene_variant | MODIFIER | c.-2241G>A| |
S1 S90 |
8 | BAA10g04750 | A10 | 2436316 | G | A | upstream_gene_variant | MODIFIER | c.-762G>A| |
S138 |
9 | BAA10g04750 | A10 | 2436402 | G | A | upstream_gene_variant | MODIFIER | c.-676G>A| |
S77 S82 |
10 | BAA10g04750 | A10 | 2437330 | C | T | intron_variant | MODIFIER | c.177+76C>T| |
S259 |
11 | BAA10g04750 | A10 | 2437388 | C | T | intron_variant | MODIFIER | c.177+134C>T| |
S146 |
12 | BAA10g04750 | A10 | 2438317 | G | A | synonymous_variant | LOW | c.342G>A|p.Glu114Glu |
S178 |
13 | BAA10g04750 | A10 | 2438575 | G | A | splice_region_variant&intron_variant | LOW | c.499+5G>A| |
S164 |
14 | BAA10g04750 | A10 | 2438813 | C | T | missense_variant | MODERATE | c.575C>T|p.Ala192Val |
S206 S26 |
15 | BAA10g04750 | A10 | 2439413 | C | T | missense_variant | MODERATE | c.851C>T|p.Ser284Phe |
S166 |
16 | BAA10g04750 | A10 | 2439626 | G | A | missense_variant | MODERATE | c.926G>A|p.Gly309Glu |
S171 |
17 | BAA10g04750 | A10 | 2440831 | G | A | splice_region_variant&synonymous_variant | LOW | c.1275G>A|p.Gln425Gln |
S234 |