Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g06130 | A06 | 3389497 | G | A | upstream_gene_variant | MODIFIER | c.-2436G>A| |
S262 |
2 | BAA06g06130 | A06 | 3392056 | C | T | stop_gained | HIGH | c.124C>T|p.Gln42* |
S221 |
3 | BAA06g06130 | A06 | 3394249 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1048-1G>A| |
S84 S93 |
4 | BAA06g06130 | A06 | 3394994 | G | A | missense_variant | MODERATE | c.1184G>A|p.Gly395Glu |
S174 S216 S27 |
5 | BAA06g06130 | A06 | 3395220 | A | C | missense_variant | MODERATE | c.1410A>C|p.Glu470Asp |
S26 S297 S306 S72 |
6 | BAA06g06130 | A06 | 3396240 | G | A | missense_variant | MODERATE | c.1922G>A|p.Arg641Lys |
S233 |
7 | BAA06g06130 | A06 | 3398108 | C | T | intron_variant | MODIFIER | c.2688+18C>T| |
S127 |
8 | BAA06g06130 | A06 | 3398533 | G | A | synonymous_variant | LOW | c.2964G>A|p.Lys988Lys |
S131 |
9 | BAA06g06130 | A06 | 3399351 | G | A | splice_donor_variant&intron_variant | HIGH | c.3228+1G>A| |
S291 |
10 | BAA06g06130 | A06 | 3399630 | G | A | missense_variant | MODERATE | c.3407G>A|p.Arg1136His |
S144 |
11 | BAA06g06130 | A06 | 3399888 | C | T | missense_variant | MODERATE | c.3584C>T|p.Ala1195Val |
S260 |
12 | BAA06g06130 | A06 | 3399898 | C | T | synonymous_variant | LOW | c.3594C>T|p.Arg1198Arg |
S210 S225 |
13 | BAA06g06130 | A06 | 3400384 | G | A | missense_variant | MODERATE | c.3908G>A|p.Cys1303Tyr |
S217 |