Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27770 | A08 | 19473486 | G | A | missense_variant | MODERATE | c.3425C>T|p.Ser1142Phe |
S259 |
2 | BAA08g27770 | A08 | 19474019 | G | A | synonymous_variant | LOW | c.2892C>T|p.Tyr964Tyr |
S23 |
3 | BAA08g27770 | A08 | 19474699 | G | A | synonymous_variant | LOW | c.2448C>T|p.Asp816Asp |
S75 S81 |
4 | BAA08g27770 | A08 | 19474898 | G | A | intron_variant | MODIFIER | c.2258-9C>T| |
S187 |
5 | BAA08g27770 | A08 | 19475722 | G | A | synonymous_variant | LOW | c.1989C>T|p.Phe663Phe |
S202 |
6 | BAA08g27770 | A08 | 19475929 | C | T | missense_variant | MODERATE | c.1867G>A|p.Glu623Lys |
S173 |
7 | BAA08g27770 | A08 | 19477003 | G | A | missense_variant | MODERATE | c.1493C>T|p.Pro498Leu |
S30 S31 |
8 | BAA08g27770 | A08 | 19477548 | C | T | synonymous_variant | LOW | c.1263G>A|p.Arg421Arg |
S47 |
9 | BAA08g27770 | A08 | 19478461 | C | T | missense_variant | MODERATE | c.350G>A|p.Gly117Glu |
S6 |
10 | BAA08g27770 | A08 | 19478595 | C | T | synonymous_variant | LOW | c.216G>A|p.Lys72Lys |
S192 |
11 | BAA08g27770 | A08 | 19479210 | G | A | upstream_gene_variant | MODIFIER | c.-149C>T| |
S225 S73 |
12 | BAA08g27770 | A08 | 19479267 | G | A | upstream_gene_variant | MODIFIER | c.-206C>T| |
S287 |
13 | BAA08g27770 | A08 | 19479322 | G | A | upstream_gene_variant | MODIFIER | c.-261C>T| |
S67 |
14 | BAA08g27770 | A08 | 19479911 | G | A | upstream_gene_variant | MODIFIER | c.-850C>T| |
S95 |
15 | BAA08g27770 | A08 | 19481923 | G | A | upstream_gene_variant | MODIFIER | c.-2862C>T| |
S234 |
16 | BAA08g27770 | A08 | 19481930 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S90 |