Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08650 | A10 | 10608241 | C | T | downstream_gene_variant | MODIFIER | c.*4748G>A| |
S168 |
2 | BAA10g08650 | A10 | 10610259 | C | T | downstream_gene_variant | MODIFIER | c.*2730G>A| |
S119 |
3 | BAA10g08650 | A10 | 10610785 | G | A | downstream_gene_variant | MODIFIER | c.*2204C>T| |
S50 |
4 | BAA10g08650 | A10 | 10611164 | C | T | downstream_gene_variant | MODIFIER | c.*1825G>A| |
S133 |
5 | BAA10g08650 | A10 | 10611821 | G | A | downstream_gene_variant | MODIFIER | c.*1168C>T| |
S105 S106 |
6 | BAA10g08650 | A10 | 10611847 | G | A | downstream_gene_variant | MODIFIER | c.*1142C>T| |
S302 |
7 | BAA10g08650 | A10 | 10612117 | C | T | downstream_gene_variant | MODIFIER | c.*872G>A| |
S235 |
8 | BAA10g08650 | A10 | 10612562 | C | T | downstream_gene_variant | MODIFIER | c.*427G>A| |
S41 |
9 | BAA10g08650 | A10 | 10614323 | G | A | missense_variant | MODERATE | c.2095C>T|p.Leu699Phe |
S283 |
10 | BAA10g08650 | A10 | 10614612 | G | A | stop_gained | HIGH | c.1918C>T|p.Gln640* |
S217 |
11 | BAA10g08650 | A10 | 10614950 | C | T | synonymous_variant | LOW | c.1725G>A|p.Gln575Gln |
S92 |
12 | BAA10g08650 | A10 | 10615331 | G | A | missense_variant | MODERATE | c.1447C>T|p.Leu483Phe |
S295 |
13 | BAA10g08650 | A10 | 10615895 | C | T | missense_variant | MODERATE | c.883G>A|p.Glu295Lys |
S183 |
14 | BAA10g08650 | A10 | 10617381 | G | A | upstream_gene_variant | MODIFIER | c.-252C>T| |
S172 |
15 | BAA10g08650 | A10 | 10617931 | G | A | upstream_gene_variant | MODIFIER | c.-802C>T| |
S18 |
16 | BAA10g08650 | A10 | 10618175 | C | T | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S162 |
17 | BAA10g08650 | A10 | 10619240 | G | A | upstream_gene_variant | MODIFIER | c.-2111C>T| |
S65 |
18 | BAA10g08650 | A10 | 10620062 | C | T | upstream_gene_variant | MODIFIER | c.-2933G>A| |
S246 |
19 | BAA10g08650 | A10 | 10621181 | G | A | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S237 |