Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05730 | A10 | 2943050 | A | G | upstream_gene_variant | MODIFIER | c.-767A>G| |
S169 S173 S225 S73 |
2 | BAA10g05730 | A10 | 2943499 | G | A | upstream_gene_variant | MODIFIER | c.-318G>A| |
S136 |
3 | BAA10g05730 | A10 | 2943828 | C | T | synonymous_variant | LOW | c.12C>T|p.Pro4Pro |
S89 |
4 | BAA10g05730 | A10 | 2944115 | C | T | missense_variant | MODERATE | c.299C>T|p.Pro100Leu |
S249 |
5 | BAA10g05730 | A10 | 2944495 | G | A | missense_variant | MODERATE | c.679G>A|p.Val227Ile |
S289 |
6 | BAA10g05730 | A10 | 2944669 | G | A | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S207 S262 |
7 | BAA10g05730 | A10 | 2944822 | C | T | synonymous_variant | LOW | c.1006C>T|p.Leu336Leu |
S10 |
8 | BAA10g05730 | A10 | 2944838 | G | A | missense_variant | MODERATE | c.1022G>A|p.Gly341Asp |
S111 |
9 | BAA10g05730 | A10 | 2944933 | G | A | missense_variant | MODERATE | c.1117G>A|p.Glu373Lys |
S172 S217 |
10 | BAA10g05730 | A10 | 2945023 | G | A | missense_variant | MODERATE | c.1207G>A|p.Val403Met |
S12 |
11 | BAA10g05730 | A10 | 2945078 | C | T | missense_variant | MODERATE | c.1262C>T|p.Pro421Leu |
S233 |
12 | BAA10g05730 | A10 | 2945396 | C | T | missense_variant | MODERATE | c.1580C>T|p.Ser527Phe |
S35 |
13 | BAA10g05730 | A10 | 2945457 | C | T | synonymous_variant | LOW | c.1641C>T|p.Ile547Ile |
S19 S305 S35 |
14 | BAA10g05730 | A10 | 2947146 | C | T | downstream_gene_variant | MODIFIER | c.*1575C>T| |
S302 |
15 | BAA10g05730 | A10 | 2947214 | G | A | downstream_gene_variant | MODIFIER | c.*1643G>A| |
S45 |
16 | BAA10g05730 | A10 | 2947766 | C | T | downstream_gene_variant | MODIFIER | c.*2195C>T| |
S260 |
17 | BAA10g05730 | A10 | 2947782 | C | T | downstream_gene_variant | MODIFIER | c.*2211C>T| |
S169 |
18 | BAA10g05730 | A10 | 2948234 | A | T | downstream_gene_variant | MODIFIER | c.*2663A>T| |
S69 |
19 | BAA10g05730 | A10 | 2949032 | G | A | downstream_gene_variant | MODIFIER | c.*3461G>A| |
S151 S263 |
20 | BAA10g05730 | A10 | 2949352 | C | T | downstream_gene_variant | MODIFIER | c.*3781C>T| |
S162 |