Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03160 | A10 | 1539538 | C | T | upstream_gene_variant | MODIFIER | c.-4856C>T| |
S271 |
2 | BAA10g03160 | A10 | 1539989 | C | T | upstream_gene_variant | MODIFIER | c.-4405C>T| |
S298 |
3 | BAA10g03160 | A10 | 1540090 | G | A | upstream_gene_variant | MODIFIER | c.-4304G>A| |
S280 |
4 | BAA10g03160 | A10 | 1543345 | G | A | upstream_gene_variant | MODIFIER | c.-1049G>A| |
S240 |
5 | BAA10g03160 | A10 | 1543389 | C | T | upstream_gene_variant | MODIFIER | c.-1005C>T| |
S28 |
6 | BAA10g03160 | A10 | 1543566 | C | T | upstream_gene_variant | MODIFIER | c.-828C>T| |
S226 |
7 | BAA10g03160 | A10 | 1544318 | C | T | upstream_gene_variant | MODIFIER | c.-76C>T| |
S37 |
8 | BAA10g03160 | A10 | 1544408 | C | T | synonymous_variant | LOW | c.15C>T|p.Ile5Ile |
S180 |
9 | BAA10g03160 | A10 | 1545283 | C | T | missense_variant | MODERATE | c.533C>T|p.Ala178Val |
S202 |
10 | BAA10g03160 | A10 | 1545349 | G | A | missense_variant | MODERATE | c.599G>A|p.Ser200Asn |
S18 |
11 | BAA10g03160 | A10 | 1548394 | T | A | downstream_gene_variant | MODIFIER | c.*2191T>A| |
S152 |
12 | BAA10g03160 | A10 | 1548681 | C | T | downstream_gene_variant | MODIFIER | c.*2478C>T| |
S104 S52 |
13 | BAA10g03160 | A10 | 1548967 | G | A | downstream_gene_variant | MODIFIER | c.*2764G>A| |
S128 |
14 | BAA10g03160 | A10 | 1549211 | G | A | downstream_gene_variant | MODIFIER | c.*3008G>A| |
S186 |