Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g30470 | A09 | 21398955 | G | A | upstream_gene_variant | MODIFIER | c.-99G>A| |
S37 |
2 | BAA09g30470 | A09 | 21399138 | G | A | missense_variant | MODERATE | c.85G>A|p.Ala29Thr |
S184 |
3 | BAA09g30470 | A09 | 21399386 | A | T | splice_acceptor_variant&intron_variant | HIGH | c.90-2A>T| |
S205 |
4 | BAA09g30470 | A09 | 21399430 | G | A | stop_gained | HIGH | c.132G>A|p.Trp44* |
S45 |
5 | BAA09g30470 | A09 | 21399676 | G | A | synonymous_variant | LOW | c.378G>A|p.Arg126Arg |
S201 |
6 | BAA09g30470 | A09 | 21399783 | G | A | missense_variant | MODERATE | c.485G>A|p.Ser162Asn |
S288 |
7 | BAA09g30470 | A09 | 21399951 | G | A | synonymous_variant | LOW | c.579G>A|p.Arg193Arg |
S182 |
8 | BAA09g30470 | A09 | 21403760 | C | A | intron_variant | MODIFIER | c.1041+2238C>A| |
S306 S308 |
9 | BAA09g30470 | A09 | 21404821 | C | A | intron_variant | MODIFIER | c.1042-2487C>A| |
S272 |
10 | BAA09g30470 | A09 | 21405071 | G | A | intron_variant | MODIFIER | c.1042-2237G>A| |
S207 |
11 | BAA09g30470 | A09 | 21406037 | G | A | intron_variant | MODIFIER | c.1042-1271G>A| |
S208 S93 |
12 | BAA09g30470 | A09 | 21406562 | G | A | intron_variant | MODIFIER | c.1042-746G>A| |
S298 |
13 | BAA09g30470 | A09 | 21406596 | G | A | intron_variant | MODIFIER | c.1042-712G>A| |
S216 |
14 | BAA09g30470 | A09 | 21406771 | G | A | intron_variant | MODIFIER | c.1042-537G>A| |
S167 |
15 | BAA09g30470 | A09 | 21407014 | C | T | intron_variant | MODIFIER | c.1042-294C>T| |
S206 S26 |
16 | BAA09g30470 | A09 | 21407092 | G | A | intron_variant | MODIFIER | c.1042-216G>A| |
S15 S3 |
17 | BAA09g30470 | A09 | 21407399 | C | T | missense_variant | MODERATE | c.1133C>T|p.Ser378Phe |
S28 |
18 | BAA09g30470 | A09 | 21407482 | G | A | missense_variant | MODERATE | c.1216G>A|p.Asp406Asn |
S185 |
19 | BAA09g30470 | A09 | 21408141 | C | T | intron_variant | MODIFIER | c.1604+22C>T| |
S191 |
20 | BAA09g30470 | A09 | 21408269 | G | A | missense_variant | MODERATE | c.1696G>A|p.Val566Ile |
S69 |
21 | BAA09g30470 | A09 | 21408296 | C | T | missense_variant | MODERATE | c.1723C>T|p.Pro575Ser |
S103 |
22 | BAA09g30470 | A09 | 21408853 | G | A | splice_region_variant&synonymous_variant | LOW | c.1785G>A|p.Ala595Ala |
S130 |
23 | BAA09g30470 | A09 | 21408881 | G | A | missense_variant | MODERATE | c.1813G>A|p.Glu605Lys |
S25 S264 |
24 | BAA09g30470 | A09 | 21408975 | G | A | missense_variant | MODERATE | c.1907G>A|p.Arg636Lys |
S110 |
25 | BAA09g30470 | A09 | 21409053 | G | A | downstream_gene_variant | MODIFIER | c.*41G>A| |
S56 |