Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18280 | A10 | 17171560 | G | A | downstream_gene_variant | MODIFIER | c.*1290C>T| |
S148 |
2 | BAA10g18280 | A10 | 17171823 | G | A | downstream_gene_variant | MODIFIER | c.*1027C>T| |
S298 |
3 | BAA10g18280 | A10 | 17172063 | C | T | downstream_gene_variant | MODIFIER | c.*787G>A| |
S48 |
4 | BAA10g18280 | A10 | 17172083 | C | T | downstream_gene_variant | MODIFIER | c.*767G>A| |
S96 |
5 | BAA10g18280 | A10 | 17172150 | G | A | downstream_gene_variant | MODIFIER | c.*700C>T| |
S132 S137 S215 |
6 | BAA10g18280 | A10 | 17172531 | G | A | downstream_gene_variant | MODIFIER | c.*319C>T| |
S262 |
7 | BAA10g18280 | A10 | 17173195 | G | A | synonymous_variant | LOW | c.2010C>T|p.Arg670Arg |
S1 S90 |
8 | BAA10g18280 | A10 | 17173467 | C | T | missense_variant | MODERATE | c.1816G>A|p.Val606Ile |
S210 |
9 | BAA10g18280 | A10 | 17174389 | C | T | synonymous_variant | LOW | c.1086G>A|p.Arg362Arg |
S44 |
10 | BAA10g18280 | A10 | 17176094 | G | A | missense_variant | MODERATE | c.182C>T|p.Pro61Leu |
S240 |
11 | BAA10g18280 | A10 | 17176408 | G | A | upstream_gene_variant | MODIFIER | c.-133C>T| |
S25 |
12 | BAA10g18280 | A10 | 17178272 | C | T | upstream_gene_variant | MODIFIER | c.-1997G>A| |
S306 S308 S78 |
13 | BAA10g18280 | A10 | 17178345 | C | T | upstream_gene_variant | MODIFIER | c.-2070G>A| |
S146 |
14 | BAA10g18280 | A10 | 17178375 | C | T | upstream_gene_variant | MODIFIER | c.-2100G>A| |
S20 |
15 | BAA10g18280 | A10 | 17181032 | A | C | upstream_gene_variant | MODIFIER | c.-4757T>G| |
S170 |