Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g14440 | A07 | 22035378 | T | A | upstream_gene_variant | MODIFIER | c.-431T>A| |
S38 |
2 | BAA07g14440 | A07 | 22035663 | C | T | upstream_gene_variant | MODIFIER | c.-146C>T| |
S116 |
3 | BAA07g14440 | A07 | 22035753 | G | A | upstream_gene_variant | MODIFIER | c.-56G>A| |
S190 |
4 | BAA07g14440 | A07 | 22035764 | C | T | upstream_gene_variant | MODIFIER | c.-45C>T| |
S262 |
5 | BAA07g14440 | A07 | 22045748 | G | A | intron_variant | MODIFIER | c.917-3098G>A| |
S80 |
6 | BAA07g14440 | A07 | 22046181 | G | A | intron_variant | MODIFIER | c.917-2665G>A| |
S201 |
7 | BAA07g14440 | A07 | 22047565 | C | T | intron_variant | MODIFIER | c.917-1281C>T| |
S148 S210 S30 |
8 | BAA07g14440 | A07 | 22047889 | C | T | intron_variant | MODIFIER | c.917-957C>T| |
S184 |
9 | BAA07g14440 | A07 | 22048001 | C | T | intron_variant | MODIFIER | c.917-845C>T| |
S149 |
10 | BAA07g14440 | A07 | 22050691 | C | T | intron_variant | MODIFIER | c.1765+490C>T| |
S235 |
11 | BAA07g14440 | A07 | 22050746 | C | T | intron_variant | MODIFIER | c.1765+545C>T| |
S143 |
12 | BAA07g14440 | A07 | 22052971 | C | T | synonymous_variant | LOW | c.2937C>T|p.Leu979Leu |
S150 |
13 | BAA07g14440 | A07 | 22053096 | C | T | missense_variant | MODERATE | c.3062C>T|p.Ala1021Val |
S32 |
14 | BAA07g14440 | A07 | 22053164 | G | A | missense_variant | MODERATE | c.3130G>A|p.Glu1044Lys |
S39 |
15 | BAA07g14440 | A07 | 22062025 | G | A | downstream_gene_variant | MODIFIER | c.*2624G>A| |
S95 |