Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07950 | A08 | 7244673 | C | T | missense_variant | MODERATE | c.2176G>A|p.Glu726Lys |
S1 S90 |
2 | BAA08g07950 | A08 | 7246965 | G | A | intron_variant | MODIFIER | c.715-210C>T| |
S219 S72 |
3 | BAA08g07950 | A08 | 7247489 | C | T | intron_variant | MODIFIER | c.714+184G>A| |
S270 |
4 | BAA08g07950 | A08 | 7247857 | C | T | missense_variant | MODERATE | c.530G>A|p.Arg177Gln |
S163 |
5 | BAA08g07950 | A08 | 7247866 | G | A | missense_variant | MODERATE | c.521C>T|p.Ala174Val |
S203 |
6 | BAA08g07950 | A08 | 7247930 | G | A | intron_variant | MODIFIER | c.475-18C>T| |
S225 S240 S73 |
7 | BAA08g07950 | A08 | 7248920 | C | T | missense_variant&splice_region_variant | MODERATE | c.316G>A|p.Gly106Arg |
S67 |
8 | BAA08g07950 | A08 | 7250946 | G | A | synonymous_variant | LOW | c.54C>T|p.Phe18Phe |
S33 |
9 | BAA08g07950 | A08 | 7250951 | G | A | missense_variant | MODERATE | c.49C>T|p.Pro17Ser |
S148 S210 |
10 | BAA08g07950 | A08 | 7251557 | C | T | upstream_gene_variant | MODIFIER | c.-558G>A| |
S56 |
11 | BAA08g07950 | A08 | 7251687 | G | A | upstream_gene_variant | MODIFIER | c.-688C>T| |
S257 |
12 | BAA08g07950 | A08 | 7251969 | C | T | upstream_gene_variant | MODIFIER | c.-970G>A| |
S144 |
13 | BAA08g07950 | A08 | 7252677 | G | A | upstream_gene_variant | MODIFIER | c.-1678C>T| |
S119 |
14 | BAA08g07950 | A08 | 7253965 | C | T | upstream_gene_variant | MODIFIER | c.-2966G>A| |
S74 |
15 | BAA08g07950 | A08 | 7254025 | G | A | upstream_gene_variant | MODIFIER | c.-3026C>T| |
S65 |
16 | BAA08g07950 | A08 | 7254102 | G | A | upstream_gene_variant | MODIFIER | c.-3103C>T| |
S181 |
17 | BAA08g07950 | A08 | 7254652 | G | A | upstream_gene_variant | MODIFIER | c.-3653C>T| |
S301 S304 |